Isolated human secreted proteins, nucleic acid molecules encoding human secreted proteins, and uses thereof

ABSTRACT

The present invention provides amino acid sequences of peptides that are encoded by genes within the human genome, the secreted peptides of the present invention. The present invention specifically provides isolated peptide and nucleic acid molecules, methods of identifying orthologs and paralogs of the secreted peptides, and methods of identifying modulators of the secreted peptides.

FIELD OF THE INVENTION

[0001] The present invention is in the field of secreted proteins that are related to the netrin-like secreted subfamily, recombinant DNA molecules, and protein production. The present invention specifically provides novel peptides and proteins that effect protein phosphorylation and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.

BACKGROUND OF THE INVENTION

[0002] Secreted Proteins

[0003] Many human proteins serve as pharmaceutically active compounds. Several classes of human proteins that serve as such active compounds include hormones, cytokines, cell growth factors, and cell differentiation factors. Most proteins that can be used as a pharmaceutically active compound fall within the family of secreted proteins. It is, therefore, important in developing new pharmaceutical compounds to identify secreted proteins that can be tested for activity in a variety of animal models. The present invention advances the state of the art by providing many novel human secreted proteins.

[0004] Secreted proteins are generally produced within cells at rough endoplasmic reticulum, are then exported to the golgi complex, and then move to secretory vesicles or granules, where they are secreted to the exterior of the cell via exocytosis.

[0005] Secreted proteins are particularly useful as diagnostic markers. Many secreted proteins are found, and can easily be measured, in serum. For example, a ‘signal sequence trap’ technique can often be utilized because many secreted proteins, such as certain secretory breast cancer proteins, contain a molecular signal sequence for cellular export. Additionally, antibodies against particular secreted serum proteins can serve as potential diagnostic agents, such as for diagnosing cancer.

[0006] Secreted proteins play a critical role in a wide array of important biological processes in humans and have numerous utilities; several illustrative examples are discussed herein. For example, fibroblast secreted proteins participate in extracellular matrix formation. Extracellular matrix affects growth factor action, cell adhesion, and cell growth. Structural and quantitative characteristics of fibroblast secreted proteins are modified during the course of cellular aging and such aging related modifications may lead to increased inhibition of cell adhesion, inhibited cell stimulation by growth factors, and inhibited cell proliferative ability (Eleftheriou et al., Mutat Res March-November 1991;256(2-6):127-38).

[0007] The secreted form of amyloid beta/A4 protein precursor (APP) functions as a growth and/or differentiation factor. The secreted form of APP can stimulate neurite extension of cultured neuroblastoma cells, presumably through binding to a cell surface receptor and thereby triggering intracellular transduction mechanisms. (Roch et al., Ann N Y Acad Sci Sep. 24, 1993;695:149-57). Secreted APPs modulate neuronal excitability, counteract effects of glutamate on growth cone behaviors, and increase synaptic complexity. The prominent effects of secreted APPs on synaptogenesis and neuronal survival suggest that secreted APPs play a major role in the process of natural cell death and, furthermore, may play a role in the development of a wide variety of neurological disorders, such as stroke, epilepsy, and Alzheimer's disease (Mattson et al., Perspect Dev Neurobiol 1998;5(4):337-52).

[0008] Breast cancer cells secrete a 52K estrogen-regulated protein (see Rochefort et al., Ann N Y Acad Sci 1986;464:190-201). This secreted protein is therefore useful in breast cancer diagnosis.

[0009] Two secreted proteins released by platelets, platelet factor 4 (PF4) and beta-thromboglobulin (betaTG), are accurate indicators of platelet involvement in hemostasis and thrombosis and assays that measure these secreted proteins are useful for studying the pathogenesis and course of thromboembolic disorders (Kaplan, Adv Exp Med Biol 1978;102:105-19).

[0010] Vascular endothelial growth factor (VEGF) is another example of a naturally secreted protein. VEGF binds to cell-surface heparan sulfates, is generated by hypoxic endothelial cells, reduces apoptosis, and binds to high-affinity receptors that are up-regulated by hypoxia (Asahara et al., Semin Interv Cardiol Sep. 1, 1996;(3):225-32).

[0011] Many critical components of the immune system are secreted proteins, such as antibodies, and many important functions of the immune system are dependent upon the action of secreted proteins. For example, Saxon et al., Biochem Soc Trans May 5, 1997;(2):383-7, discusses secreted IgE proteins.

[0012] For a further review of secreted proteins, see Nilsen-Hamilton et al., Cell Biol Int Rep September 1982 6;(9):815-36.

[0013] Netrins

[0014] Experimental evidence has demonstrated that the netrin family of proteins are involved in embryonic nervous system development in both vertebrates and invertebrates. Specifically, they have been shown to provide guidance for developing axons. Tessier-Lavigne and Goodman, Science 274:1123-1133, (1996). For example, Netrin-1, a diffusable protein made by floor plate cells, has been shown to attract spinal commissural axons and repel trochlear axons in vitro, as well as play a vital role in mouse neuron development. Serafini, et al., Cell 87:1001-1014, (1996). Netrin has been shown to interact with a laminin protein to convert netrin-mediated attraction into repulsion. It has been suggested that repulsion from the region in which laminin and netrin are coexpressed may help to drive axons into the region where only netrin is present, providing a mechanism for their escape from the regions such as the retinal surface. Hopker, et al., Nature 401:69-73, (1999). Experimental evidence suggests that netrin provides guidance for axons by activating the neuronal DCC receptor, and that chemical inhibitors of metalloproteases increase netrin-mediated axon growth in vitro. Galko and Tessier-Lavigne, Science 289:1365-1367, (2000).

[0015] Netrin-G1 is a member of the netrin family, but unlike typical netrins, netrin-G1 consists of at least six isoforms of which five were predominantly anchored to the plasma membrane via glycosyl phosphatidyl-inositol linkages. Netrin-G1 transcripts are expressed in mouse in midbrain and hindbrain regions by embryonic day 12, and reach their highest levels of expression at perinatal stages in various brain regions, including olfactory bulb mitral cells, thalamus, and deep cerebellar nuclei. Unlike typical netrin proteins, netrin-G1 proteins did not show appreciable affinity to any netrin receptor examined. Unlike netrin-1, secreted netrin-G1 does not attract circumferentially growing axons from the cerebellar plate. The expression pattern of netrin-G1 and its predicted neuronal membrane localization suggest it may also have novel signaling functions in nervous system development. For more information on Netrin-G1, see Nakashiba, et al., J Neurosci September 1;20(17):6540-50 (2000).

[0016] Secreted proteins, particularly members of the netrin-like secreted protein subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown members of this subfamily of secreted proteins. The present invention advances the state of the art by providing previously unidentified human secreted proteins that have homology to members of the netrin-like secreted protein subfamily.

SUMMARY OF THE INVENTION

[0017] The present invention is based in part on the identification of amino acid sequences of human secreted peptides and proteins that are related to the netrin-like secreted protein subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate secreted protein activity in cells and tissues that express the secreted protein. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma.

DESCRIPTION OF THE FIGURE SHEETS

[0018]FIG. 1 provides the nucleotide sequence of a cDNA molecule or transcript sequence that encodes the secreted protein of the present invention. (SEQ ID NO: 1) In addition, structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma.

[0019]FIG. 2 provides the predicted amino acid sequence of the secreted protein of the present invention. (SEQ ID NO: 2) In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.

[0020]FIG. 3 provides genomic sequences that span the gene encoding the secreted protein of the present invention. (SEQ ID NO: 3) In addition structure and functional information, such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence. As illustrated in FIG. 3, SNPs were identified at 90 different nucleotide positions.

DETAILED DESCRIPTION OF THE INVENTION

[0021] General Description

[0022] The present invention is based on the sequencing of the human genome. During the sequencing and assembly of the human genome, analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a secreted protein or part of a secreted protein and are related to the netrin-like secreted protein subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized. Based on this analysis, the present invention provides amino acid sequences of human secreted peptides and proteins that are related to the netrin-like secreted protein subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these secreted peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the secreted protein of the present invention.

[0023] In addition to being previously unknown, the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known secreted proteins of the netrin-like secreted protein subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene. Some of the more specific features of the peptides of the present invention, and the uses thereof, are described herein, particularly in the Background of the Invention and in the annotation provided in the Figures, and/or are known within the art for each of the known netrin-like family or subfamily of secreted proteins.

SPECIFIC EMBODIMENTS

[0024] Peptide Molecules

[0025] The present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the secreted protein family of proteins and are related to the netrin-like secreted protein subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIG. 1 and genomic sequences are provided in FIG. 3). The peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the secreted peptides of the present invention, secreted peptides, or peptides/proteins of the present invention.

[0026] The present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprise the amino acid sequences of the secreted peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.

[0027] As used herein, a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals. The peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).

[0028] In some uses, “substantially free of cellular material” includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins. When the peptide is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.

[0029] The language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the secreted peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.

[0030] The isolated secreted peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. For example, a nucleic acid molecule encoding the secreted peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell. The protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.

[0031] Accordingly, the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO: 2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO: 1) and the genomic sequences provided in FIG. 3 (SEQ ID NO: 3). The amino acid sequence of such a protein is provided in FIG. 2. A protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.

[0032] The present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO: 2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO: 1) and the genomic sequences provided in FIG. 3 (SEQ ID NO: 3). A protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.

[0033] The present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO: 2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO: 1) and the genomic sequences provided in FIG. 3 (SEQ ID NO: 3). A protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids. The preferred classes of proteins that are comprised of the secreted peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.

[0034] The secreted peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins. Such chimeric and fusion proteins comprise a secreted peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the secreted peptide. “Operatively linked” indicates that the secreted peptide and the heterologous protein are fused in-frame. The heterologous protein can be fused to the N-terminus or C-terminus of the secreted peptide.

[0035] In some uses, the fusion protein does not affect the activity of the secreted peptide per se. For example, the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions. Such fusion proteins, particularly poly-His fusions, can facilitate the purification of recombinant secreted peptide. In certain host cells (e.g., mammalian host cells), expression and/or secretion of a protein can be increased by using a heterologous signal sequence.

[0036] A chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al., Current Protocols in Molecular Biology, 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein). A secreted peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the secreted peptide.

[0037] As mentioned above, the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides. Such variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.

[0038] Such variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the secreted peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.

[0039] To determine the percent identity of two amino acid sequences or two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). In a preferred embodiment, at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of the length of a reference sequence is aligned for comparison purposes. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.

[0040] The comparison of sequences and determination of percent identity and similarity between two sequences can be accomplished using a mathematical algorithm. (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part 1, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991). In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package (available at http://www.gcg.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)) (available at http://www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.

[0041] The nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. (J. Mol. Biol. 215:403-10 (1990)). BLAST nucleotide searches can be performed with the NBLAST program, score=100, wordlength=12 to obtain nucleotide sequences homologous to the nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST program, score=50, wordlength=3 to obtain amino acid sequences homologous to the proteins of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (Nucleic Acids Res. 25(17):3389-3402 (1997)). When utilizing BLAST and gapped BLAST programs, the default parameters of the respective programs (e.g., XBLAST and NBLAST) can be used.

[0042] Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the secreted peptides of the present invention as well as being encoded by the same genetic locus as the secreted peptide provided herein.

[0043] Allelic variants of a secreted peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the secreted peptide as well as being encoded by the same genetic locus as the secreted peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. As used herein, two proteins (or a region of the proteins) have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous. A significantly homologous amino acid sequence, according to the present invention, will be encoded by a nucleic acid sequence that will hybridize to a secreted peptide encoding nucleic acid molecule under stringent conditions as more fully described below.

[0044]FIG. 3 provides information on SNPs that have been found in the gene encoding the receptor protein of the present invention. SNPs were identified at 90 different nucleotide positions, including a non-synonymous coding SNP at positions 753666 and 75368. Changes in the amino acid sequence caused by these SNPs is indicated in FIG. 3 and can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. Some of these SNPs that are located outside the ORF and in introns may affect gene expression. Positioning of each SNP in an exon, intron, or outside the ORF can readily be determined using the DNA position given for each SNP and the start/stop, exon, and intron genomic coordinates given in FIG. 3.

[0045] Paralogs of a secreted peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the secreted peptide, as being encoded by a gene from humans, and as having similar activity or function. Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain. Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a secreted peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.

[0046] Orthologs of a secreted peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the secreted peptide as well as being encoded by a gene from another organism. Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents. Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a secreted peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins.

[0047] Non-naturally occurring variants of the secreted peptides of the present invention can readily be generated using recombinant techniques. Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the secreted peptide. For example, one class of substitutions are conserved amino acid substitution. Such substitutions are those that substitute a given amino acid in a secreted peptide by another amino acid of like characteristics. Typically seen as conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr. Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al., Science 247:1306-1310 (1990).

[0048] Variant secreted peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind substrate, ability to phosphorylate substrate, ability to mediate signaling, etc. Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions. FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions. Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.

[0049] Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.

[0050] Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al., Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2. The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as secreted protein activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al., J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).

[0051] The present invention further provides fragments of the secreted peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2. The fragments to which the invention pertains, however, are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.

[0052] As used herein, a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a secreted peptide. Such fragments can be chosen based on the ability to retain one or more of the biological activities of the secreted peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen. Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length. Such fragments will typically comprise a domain or motif of the secreted peptide, e.g., active site or a substrate-binding domain. Further, possible fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures. Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2.

[0053] Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the termninal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in secreted peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2).

[0054] Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.

[0055] Such modifications are well known to those of skill in the art and have been described in great detail in the scientific literature. Several particularly common modifications, glycosylation, lipid attachment, sulfation, gamma-carboxylation of glutarnic acid residues, hydroxylation and ADP-ribosylation, for instance, are described in most basic texts, such as Proteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993). Many detailed reviews are available on this subject, such as by Wold, F., Posttranslational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York 1-12 (1983); Seifter et al. (Meth. Enzymol. 182:626-646 (1990)) and Rattan et al. (Ann. N.Y. Acad. Sci. 663:48-62 (1992)).

[0056] Accordingly, the secreted peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature secreted peptide is fused with another compound, such as a compound to increase the half-life of the secreted peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature secreted peptide, such as a leader or secretory sequence or a sequence for purification of the mature secreted peptide or a pro-protein sequence.

[0057] Protein/Peptide Uses

[0058] The proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state). Where the protein binds or potentially binds to another protein or ligand (such as, for example, in a secreted protein-effector protein interaction or secreted protein-ligand interaction), the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.

[0059] Methods for performing the uses listed above are well known to those skilled in the art. References disclosing such methods include “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds., 1989, and “Methods in Enzymology: Guide to Molecular Cloning Techniques”, Academic Press, Berger, S. L. and A. R. Kimmel eds., 1987.

[0060] The potential uses of the peptides of the present invention are based primarily on the source of the protein as well as the class/action of the protein. For example, secreted proteins isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the secreted protein. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma. A large percentage of pharmaceutical agents are being developed that modulate the activity of secreted proteins, particularly members of the netrin-like subfamily (see Background of the Invention). The structural and functional information provided in the Background and Figures provide specific and substantial uses for the molecules of the present invention, particularly in combination with the expression information provided in FIG. 1. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. Such uses can readily be determined using the information provided herein, that which is known in the art, and routine experimentation.

[0061] The proteins of the present invention (including variants and fragments that may have been disclosed prior to the present invention) are useful for biological assays related to secreted proteins that are related to members of the netrin-like subfamily. Such assays involve any of the known secreted protein functions or activities or properties useful for diagnosis and treatment of secreted protein-related conditions that are specific for the subfamily of secreted proteins that the one of the present invention belongs to, particularly in cells and tissues that express the secreted protein. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma.

[0062] The proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems. Cell-based systems can be native, i.e., cells that normally express the secreted protein, as a biopsy or expanded in cell culture. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. In an alternate embodiment, cell-based assays involve recombinant host cells expressing the secreted protein.

[0063] The polypeptides can be used to identify compounds that modulate secreted protein activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the secreted protein. Both the secreted proteins of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the secreted protein. These compounds can be further screened against a functional secreted protein to determine the effect of the compound on the secreted protein activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the secreted protein to a desired degree.

[0064] Further, the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the secreted protein and a molecule that normally interacts with the secreted protein, e.g. a substrate or a component of the signal pathway that the secreted protein normally interacts (for example, another secreted protein). Such assays typically include the steps of combining the secreted protein with a candidate compound under conditions that allow the secreted protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the secreted protein and the target.

[0065] Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al., Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L- configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′)₂, Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic molecules (e.g., molecules obtained from combinatorial and natural product libraries).

[0066] One candidate compound is a soluble fragment of the receptor that competes for substrate binding. Other candidate compounds include mutant secreted proteins or appropriate fragments containing mutations that affect secreted protein function and thus compete for substrate. Accordingly, a fragment that competes for substrate, for example with a higher affinity, or a fragment that binds substrate but does not allow release, is encompassed by the invention.

[0067] Any of the biological or biochemical functions mediated by the secreted protein can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2. Specifically, a biological function of a cell or tissues that expresses the secreted protein can be assayed. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma.

[0068] Binding and/or activating compounds can also be screened by using chimeric secreted proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions. For example, a substrate-binding region can be used that interacts with a different substrate then that which is recognized by the native secreted protein. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the secreted protein is derived.

[0069] The proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the secreted protein (e.g. binding partners and/or ligands). Thus, a compound is exposed to a secreted protein polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide. Soluble secreted protein polypeptide is also added to the mixture. If the test compound interacts with the soluble secreted protein polypeptide, it decreases the amount of complex formed or activity from the secreted protein target. This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the secreted protein. Thus, the soluble polypeptide that competes with the target secreted protein region is designed to contain peptide sequences corresponding to the region of interest.

[0070] To perform cell free drug screening assays, it is sometimes desirable to immobilize either the secreted protein, or fragment, or its target molecule to facilitate separation of complexes from uncomplexed forms of one or both of the proteins, as well as to accommodate automation of the assay.

[0071] Techniques for immobilizing proteins on matrices can be used in the drug screening assays. In one embodiment, a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix. For example, glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtitre plates, which are then combined with the cell lysates (e.g., ³⁵S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated. Alternatively, the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of secreted protein-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques. For example, either the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art. Alternatively, antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation. Preparations of a secreted protein-binding protein and a candidate compound are incubated in the secreted protein-presenting wells and the amount of complex trapped in the well can be quantitated. Methods for detecting such complexes, in addition to those described above for the GST-immobilized complexes, include immunodetection of complexes using antibodies reactive with the secreted protein target molecule, or which are reactive with secreted protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.

[0072] Agents that modulate one of the secreted proteins of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.

[0073] Modulators of secreted protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the secreted protein pathway, by treating cells or tissues that express the secreted protein. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. These methods of treatment include the steps of administering a modulator of secreted protein activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.

[0074] In yet another aspect of the invention, the secreted proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al. (1993) Cell 72:223-232; Madura et al. (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al. (1993) Oncogene 8:1693-1696; and Brent WO94/10300), to identify other proteins, which bind to or interact with the secreted protein and are involved in secreted protein activity.

[0075] The two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. Briefly, the assay utilizes two different DNA constructs. In one construct, the gene that codes for a secreted protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4). In the other construct, a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor. If the “bait” and the “prey” proteins are able to interact, in vivo, forming a secreted protein-dependent complex, the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the secreted protein.

[0076] This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent identified as described herein (e.g., a secreted protein-modulating agent, an antisense secreted protein nucleic acid molecule, a secreted protein-specific antibody, or a secreted protein-binding partner) can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent. Alternatively, an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.

[0077] The secreted proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. The method involves contacting a biological sample with a compound capable of interacting with the secreted protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.

[0078] One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein. A biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.

[0079] The peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs. Thus, the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification. Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered secreted protein activity in cell-based or cell-free assay, alteration in substrate or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.

[0080] In vitro techniques for detection of peptide include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent. Alternatively, the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.

[0081] The peptides are also useful in pharmacogenomic analysis. Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. (Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. (Clin. Chem. 43(2):254-266 (1997)). The clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism. Thus, the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound. Further, the activity of drug metabolizing enzymes effects both the intensity and duration of drug action. Thus, the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype. The discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer. Accordingly, genetic polymorphism may lead to allelic protein variants of the secreted protein in which one or more of the secreted protein functions in one population is different from those in another population. The peptides thus allow a target to ascertain a genetic predisposition that can affect treatment modality. Thus, in a ligand-based treatment, polymorphism may give rise to amino terminal extracellular domains and/or other substrate-binding regions that are more or less active in substrate binding, and secreted protein activation. Accordingly, substrate dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism. As an alternative to genotyping, specific polymorphic peptides could be identified.

[0082] The peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. Accordingly, methods for treatment include the use of the secreted protein or fragments.

[0083] Antibodies

[0084] The invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof. As used herein, an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins. An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.

[0085] As used herein, an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge. The antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′)₂, and Fv fragments.

[0086] Many methods are known for generating and/or identifying antibodies to a given target peptide. Several such methods are described by Harlow, Antibodies, Cold Spring Harbor Press, (1989).

[0087] In general, to generate antibodies, an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse. The full-length protein, an antigenic peptide fragment or a fusion protein can be used. Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.

[0088] Antibodies are preferably prepared from regions or discrete fragments of the secreted proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or secreted protein/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.

[0089] An antigenic fragment will typically comprise at least 8 contiguous amino acid residues. The antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues. Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2).

[0090] Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, β-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidinibiotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include ¹²⁵I, ¹³¹i, ³⁵S or ³H.

[0091] Antibody Uses

[0092] The antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation. The antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells. In addition, such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma. Further, such antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression. Also, such antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition. Antibody detection of circulating fragments of the full length protein can be used to identify turnover.

[0093] Further, the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function. When a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form, the antibody can be prepared against the normal protein. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.

[0094] The antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. The diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.

[0095] Additionally, antibodies are useful in pharmacogenomic analysis. Thus, antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities. The antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.

[0096] The antibodies are also useful for tissue typing. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. Thus, where a specific protein has been correlated with expression in a specific tissue, antibodies that are specific for this protein can be used to identify a tissue type.

[0097] The antibodies are also useful for inhibiting protein function, for example, blocking the binding of the secreted peptide to a binding partner such as a substrate. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function. An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity. Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.

[0098] The invention also encompasses kits for using antibodies to detect the presence of a protein in a biological sample. The kit can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use. Such a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nuleic acid arrays and similar methods have been developed for antibody arrays.

[0099] Nucleic Acid Molecules

[0100] The present invention further provides isolated nucleic acid molecules that encode a secreted peptide or protein of the present invention (cDNA, transcript and genomic sequence). Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the secreted peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.

[0101] As used herein, an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid. Preferably, an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. However, there can be some flanking nucleotide sequences, for example up to about 5KB, 4KB, 3KB, 2KB, or 1KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence. The important point is that the nucleic acid is isolated from remote and unimportant flanking sequences such that it can be subjected to the specific manipulations described herein such as recombinant expression, preparation of probes and primers, and other uses specific to the nucleic acid sequences.

[0102] Moreover, an “isolated” nucleic acid molecule, such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized. However, the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.

[0103] For example, recombinant DNA molecules contained in a vector are considered isolated. Further examples of isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution. Isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention. Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.

[0104] Accordingly, the present invention provides nucleic acid molecules that consist of the nucleotide sequence shown in FIGS. 1 or 3 (SEQ ID NO: 1, transcript sequence and SEQ ID NO: 3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO: 2. A nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.

[0105] The present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIGS. 1 or 3 (SEQ ID NO: 1, transcript sequence and a SEQ ID NO: 3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO: 2. A nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.

[0106] The present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIGS. 1 or 3 (SEQ ID NO: 1, transcript sequence and SEQ ID NO: 3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO: 2. A nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule. In such a fashion, the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences. Such a nucleic acid molecule can have a few additional nucleotides or can comprises several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.

[0107] In FIGS. 1 and 3, both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.

[0108] The isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.

[0109] As mentioned above, the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the secreted peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA. In addition, the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.

[0110] Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof. The nucleic acid, especially DNA, can be double-stranded or single-stranded. Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).

[0111] The invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the secreted proteins of the present invention that are described above. Such nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis. Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.

[0112] The present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3. Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents. A promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3.

[0113] A fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a CDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.

[0114] A probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.

[0115] Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene.

[0116]FIG. 3 provides information on SNPs that have been found in the gene encoding the receptor protein of the present invention. SNPs were identified at 90 different nucleotide positions, including a non-synonymous coding SNP at positions 753666 and 75368. Changes in the amino acid sequence caused by these SNPs is indicated in FIG. 3 and can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. Some of these SNPs that are located outside the ORF and in introns may affect gene expression. Positioning of each SNP in an exon, intron, or outside the ORF can readily be determined using the DNA position given for each SNP and the start/stop, exon, and intron genomic coordinates given in FIG. 3.

[0117] As used herein, the term “hybridizes under stringent conditions” is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other. The conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. One example of stringent hybridization conditions are hybridization in 6× sodium chloride/sodium citrate (SSC) at about 45C, followed by one or more washes in 0.2×SSC, 0.1% SDS at 50-65C. Examples of moderate to low stringency hybridization conditions are well known in the art.

[0118] Nucleic Acid Molecule Uses

[0119] The nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays. The nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2. As illustrated in FIG. 3, SNPs were identified at 90 different nucleotide positions.

[0120] The probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.

[0121] The nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.

[0122] The nucleic acid molecules are also useful for constructing recombinant vectors. Such vectors include expression vectors that express a portion of, or all of, the peptide sequences. Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product. For example, an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.

[0123] The nucleic acid molecules are also useful for expressing antigenic portions of the proteins.

[0124] The nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods.

[0125] The nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.

[0126] The nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.

[0127] The nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.

[0128] The nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.

[0129] The nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.

[0130] The nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma. Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms. The nucleic acid whose level is determined can be DNA or RNA. Accordingly, probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in secreted protein expression relative to normal results.

[0131] In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detecting DNA include Southern hybridizations and in situ hybridization.

[0132] Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a secreted protein, such as by measuring a level of a secreted protein-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a secreted protein gene has been mutated. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma.

[0133] Nucleic acid expression assays are useful for drug screening to identify compounds that modulate secreted protein nucleic acid expression.

[0134] The invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the secreted protein gene, particularly biological and pathological processes that are mediated by the secreted protein in cells and tissues that express it. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma. The method typically includes assaying the ability of the compound to modulate the expression of the secreted protein nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired secreted protein nucleic acid expression. The assays can be performed in cell-based and cell-free systems. Cell-based assays include cells naturally expressing the secreted protein nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.

[0135] Thus, modulators of secreted protein gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined. The level of expression of secreted protein mRNA in the presence of the candidate compound is compared to the level of expression of secreted protein mRNA in the absence of the candidate compound. The candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression. When expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression. When nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.

[0136] The invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate secreted protein nucleic acid expression in cells and tissues that express the secreted protein. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.

[0137] Alternatively, a modulator for secreted protein nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the secreted protein nucleic acid expression in the cells and tissues that express the protein. Experimental data as provided in FIG. 1 indicates expression in glioblastoma and adrenal cortex carcinoma.

[0138] The nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the secreted protein gene in clinical trials or in a treatment regimen. Thus, the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance. The gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.

[0139] The nucleic acid molecules are also useful in diagnostic assays for qualitative changes in secreted protein nucleic acid expression, and particularly in qualitative changes that lead to pathology. The nucleic acid molecules can be used to detect mutations in secreted protein genes and gene expression products such as mRNA. The nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the secreted protein gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the secreted protein gene associated with a dysfunction provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a secreted protein.

[0140] Individuals carrying mutations in the secreted protein gene can be detected at the nucleic acid level by a variety of techniques. FIG. 3 provides information on SNPs that have been found in the gene encoding the receptor protein of the present invention. SNPs were identified at 90 different nucleotide positions, including a non-synonymous coding SNP at positions 753666 and 75368. Changes in the amino acid sequence caused by these SNPs is indicated in FIG. 3 and can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. Some of these SNPs that are located outside the ORF and in introns may affect gene expression. Positioning of each SNP in an exon, intron, or outside the ORF can readily be determined using the DNA position given for each SNP and the start/stop, exon, and intron genomic coordinates given in FIG. 3. Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis. RNA or cDNA can be used in the same way. In some uses, detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos. 4,683,195 and 4,683,202), such as anchor PCR or RACE PCR, or, alternatively, in a ligation chain reaction (LCR) (see, e.g., Landegran et al., Science 241:1077-1080 (1988); and Nakazawa et al., PNAS 91:360-364 (1994)), the latter of which can be particularly useful for detecting point mutations in the gene (see Abravaya et al., Nucleic Acids Res. 23:675-682 (1995)). This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, “mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences.

[0141] Alternatively, mutations in a secreted protein gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.

[0142] Further, sequence-specific ribozymes (U.S. Pat. No. 5,498,531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.

[0143] Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and SI protection or the chemical cleavage method. Furthermore, sequence differences between a mutant secreted protein gene and a wild-type gene can be determined by direct DNA sequencing. A variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995) Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al., Appl. Biochem. BiotechnoL 38:147-159 (1993)).

[0144] Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al., Science 230:1242 (1985)); Cotton et al, PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144(1993); and Hayashi et al., Genet. Anal. Tech. Appl. 9:73-79 (1992)), and movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (Myers et al., Nature 313:495 (1985)). Examples of other techniques for detecting point mutations include selective oligonucleotide hybridization, selective amplification, and selective primer extension.

[0145] The nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality. Thus, the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship). Accordingly, the nucleic acid molecules described herein can be used to assess the mutation content of the secreted protein gene in an individual in order to select an appropriate compound or dosage regimen for treatment. FIG. 3 provides information on SNPs that have been found in the gene encoding the receptor protein of the present invention. SNPs were identified at 90 different nucleotide positions, including a non-synonymous coding SNP at positions 753666 and 75368. Changes in the amino acid sequence caused by these SNPs is indicated in FIG. 3 and can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. Some of these SNPs that are located outside the ORF and in introns may affect gene expression. Positioning of each SNP in an exon, intron, or outside the ORF can readily be determined using the DNA position given for each SNP and the start/stop, exon, and intron genomic coordinates given in FIG. 3.

[0146] Thus nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.

[0147] The nucleic acid molecules are thus useful as antisense constructs to control secreted protein gene expression in cells, tissues, and organisms. A DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of secreted protein. An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into secreted protein.

[0148] Alternatively, a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of secreted protein nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired secreted protein nucleic acid expression. This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the secreted protein, such as substrate binding.

[0149] The nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in secreted protein gene expression. Thus, recombinant cells, which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired secreted protein to treat the individual.

[0150] The invention also encompasses kits for detecting the presence of a secreted protein nucleic acid in a biological sample. Experimental data as provided in FIG. 1 indicates that secreted proteins of the present invention are expressed in glioblastoma and adrenal cortex carcinoma. Specifically, a virtual northern blot shows expression in glioblastoma and adrenal cortex carcinoma. For example, the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting secreted protein nucleic acid in a biological sample; means for determining the amount of secreted protein nucleic acid in the sample; and means for comparing the amount of secreted protein nucleic acid in the sample with a standard. The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect secreted protein mRNA or DNA.

[0151] Nucleic Acid Arrays

[0152] The present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).

[0153] As used herein “Arrays” or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support. In one embodiment, the microarray is prepared and used according to the methods described in U.S. Pat. No. 5,837,832, Chee et al., PCT application W095/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et al. (1996; Proc. Natl. Acad. Sci. 93:10614-10619), all of which are incorporated herein in their entirety by reference. In other embodiments, such arrays are produced by the methods described by Brown et al., U.S. Pat. No. 5,807,522.

[0154] The microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support. The oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length. The microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides which cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence. Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.

[0155] In order to produce oligonucleotides to a known sequence for a microarray or detection kit, the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit. The “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence. The second oligonucleotide in the pair (mismatched by one) serves as a control. The number of oligonucleotide pairs may range from two to one million. The oligomers are synthesized at designated areas on a substrate using a light-directed chemical process. The substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.

[0156] In another aspect, an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application W095/25 1116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference. In another aspect, a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures. An array, such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.

[0157] In order to conduct sample analysis using a microarray or detection kit, the RNA or DNA from a biological sample is made into hybridization probes. The mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA). The aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence. The scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit. The biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations. A detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.

[0158] Using such arrays, the present invention provides methods to identify the expression of the secreted proteins/peptides of the present invention. In detail, such methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample. Such assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the secreted protein gene of the present invention. FIG. 3 provides information on SNPs that have been found in the gene encoding the receptor protein of the present invention. SNPs were identified at 90 different nucleotide positions, including a non-synonymous coding SNP at positions 753666 and 75368. Changes in the amino acid sequence caused by these SNPs is indicated in FIG. 3 and can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. Some of these SNPs that are located outside the ORF and in introns may affect gene expression. Positioning of each SNP in an exon, intron, or outside the ORF can readily be determined using the DNA position given for each SNP and the start/stop, exon, and intron genomic coordinates given in FIG. 3.

[0159] Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay. One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T, An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Lab oratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).

[0160] The test samples of the present invention include cells, protein or membrane extracts of cells. The test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.

[0161] In another embodiment of the present invention, kits are provided which contain the necessary reagents to carry out the assays of the present invention.

[0162] Specifically, the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.

[0163] In detail, a compartmentalized kit includes any kit in which reagents are contained in separate containers. Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica. Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another. Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe. One skilled in the art will readily recognize that the previously unidentified secreted protein gene of the present invention can be routinely identified using the sequence information disclosed herein can be readily incorporated into one of the established kit formats which are well known in the art, particularly expression arrays.

[0164] Vectors/host cells

[0165] The invention also provides vectors containing the nucleic acid molecules described herein. The term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules. When the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid. With this aspect of the invention, the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.

[0166] A vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules. Alternatively, the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.

[0167] The invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules. The vectors can function in prokarvotic or eukaryotic cells or in both (shuttle vectors).

[0168] Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell. The nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription. Thus, the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector. Alternatively, a trans-acting factor may be supplied by the host cell. Finally, a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.

[0169] The regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage λ, the lac, TRP, and TAC promoters from E. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.

[0170] In addition to control regions that promote transcription, expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers. Examples include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.

[0171] In addition to containing sites for transcription initiation and control, expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation. Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals. The person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).

[0172] A variety of expression vectors can be used to express a nucleic acid molecule. Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses. Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g. cosmids and phagemids. Appropriate cloning and expression vectors for prokaryotic and eukaryotic hosts are described in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).

[0173] The regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand. A variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.

[0174] The nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology. Generally, the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.

[0175] The vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques. Bacterial cells include, but are not limited to, E. coli, Streptomyces, and Salmonella typhimurium. Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.

[0176] As described herein, it may be desirable to express the peptide as a fusion protein. Accordingly, the invention provides fusion vectors that allow for the production of the peptides. Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification. A proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety. Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enterokinase. Typical fusion expression vectors include pGEX (Smith et al., Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein. Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).

[0177] Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein. (Gottesman, S., Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990)119-128). Alternatively, the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al., Nucleic Acids Res. 20:2111-2118 (1992)).

[0178] The nucleic acid molecules can also be expressed by expression vectors that are operative in yeast. Examples of vectors for expression in yeast e.g., S. cerevisiae include pYepSec1 (Baldari, et al., EMBO J. 6:229-234 (1987)), pMFa (Kuijan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).

[0179] The nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g., Sf 9 cells) include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al., Virology 170:31-39 (1989)).

[0180] In certain embodiments of the invention, the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors. Examples of mammalian expression vectors include pCDM8 (Seed, B. Nature 329:840(1987)) and pMT2PC (Kaufman et al., EMBO J. 6:187-195 (1987)).

[0181] The expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules. The person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.

[0182] The invention also encompasses vectors in which the nucleic acid sequences described herein are cloned into the vector in reverse orientation, but operably linked to a regulatory sequence that permits transcription of antisense RNA. Thus, an antisense transcript can be produced to all, or to a portion, of the nucleic acid molecule sequences described herein, including both coding and non-coding regions. Expression of this antisense RNA is subject to each of the parameters described above in relation to expression of the sense RNA (regulatory sequences, constitutive or inducible expression, tissue-specific expression).

[0183] The invention also relates to recombinant host cells containing the vectors described herein. Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.

[0184] The recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. (Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).

[0185] Host cells can contain more than one vector. Thus, different nucleotide sequences can be introduced on different vectors of the same cell. Similarly, the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors. When more than one vector is introduced into a cell, the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.

[0186] In the case of bacteriophage and viral vectors, these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction. Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.

[0187] Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs. The marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.

[0188] While the mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell- free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.

[0189] Where secretion of the peptide is desired, which is difficult to achieve with multi-transmembrane domain containing proteins such as kinases, appropriate secretion signals are incorporated into the vector. The signal sequence can be endogenous to the peptides or heterologous to these peptides.

[0190] Where the peptide is not secreted into the medium, which is typically the case with kinases, the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like. The peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatite chromatography, lectin chromatography, or high performance liquid chromatography.

[0191] It is also understood that depending upon the host cell in recombinant production of the peptides described herein, the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria. In addition, the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.

[0192] Uses of vectors and host cells

[0193] The recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a secreted protein or peptide that can be further purified to produce desired amounts of secreted protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.

[0194] Host cells are also useful for conducting cell-based assays involving the secreted protein or secreted protein fragments, such as those described above as well as other formats known in the art. Thus, a recombinant host cell expressing a native secreted protein is useful for assaying compounds that stimulate or inhibit secreted protein function.

[0195] Host cells are also useful for identifying secreted protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant secreted protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native secreted protein.

[0196] Genetically engineered host cells can be further used to produce non-human transgenic animals. A transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene. A transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a secreted protein and identifying and evaluating modulators of secreted protein activity. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.

[0197] A transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal. Any of the secreted protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.

[0198] Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included. A tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the secreted protein to particular cells.

[0199] Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al., U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B., Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes. A transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.

[0200] In another embodiment, transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage P1. For a description of the cre/loxP recombinase system, see, e.g., Lakso et al. PNAS 89:6232-6236 (1992). Another example of a recombinase system is the FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991). If a cre/loxP recombinase system is used to regulate expression of the transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein is required. Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.

[0201] Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al. Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669. In brief, a cell, e.g., a somatic cell, from the transgenic animal can be isolated and induced to exit the growth cycle and enter G₀ phase. The quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal. The offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.

[0202] Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect substrate binding, secreted protein activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo secreted protein function, including substrate interaction, the effect of specific mutant secreted proteins on secreted protein function and substrate interaction, and the effect of chimeric secreted proteins. It is also possible to assess the effect of null mutations, that is, mutations that substantially or completely eliminate one or more secreted protein functions.

[0203] All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the above-described modes for carrying out the invention which are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims.

1 5 1 3537 DNA Human 1 ttggtgatcg tgagtgatgg caagaggatt tagcctcggc attaacttgg agcggagtgc 60 aggggggcag tgaagcgccc gccatctggc ccgcgccgcg ccggggggat gccccggctc 120 cccgacgaga cgccgcgaag cccacccggg ccgggggctg cccggcgccc gagcgcgggt 180 cctccccggg ccgcccaggg gggccaaaaa gtttgcactt gttagcggcg acctcccgct 240 cagcccgggc gggcgatgcg ggcggcgcgg gcggccccct cccccggccc gcgtctccgg 300 gacggctgcg ggcggccccc ccggcggccg gagggctccc tggccccgat ctgacggcgg 360 cggcggcggc ggccacagcg gcgggagcgg cgcggggaag gagcagcggc tcgcagccct 420 cggcccgcgc ccccacccag cgccagcccg aggggggagg cgcagcgccg gagggtggcg 480 gtcctcggcc ctcccaggtc tccgcgccgg gaagccgctc cgagccggga ttgtgcctat 540 gattgggggg ctgtttctca gtgcctggct cttcatggtt ggccagcacg tggagcactc 600 tgttcatctg tacatataga caagtcagac cccaggtacc tggatggatt gagagctgag 660 atctcagaaa cttcataata agttgccgat ggctaccagc caaggctgga gggttgtttt 720 gccgttgtgt tgagcacgtc acccattaag agccctttaa agacctggat tgattggaag 780 gacaaaaatt aaaagcaatc tgatccagcc tcatgcagga tccctgcgga ttttctcctt 840 atcccatttc catccactgt cacaatttga gaatctgcct gatttgatca gattcacctc 900 caggggaggt gtgataccag ggttaggagg acgtgaagtt atgggcaact ttctgatctg 960 tccatcagca gtctgagaaa cgctggctct gaattttccg tgtcggcctt ttggaaacaa 1020 caagttcctc gctgtttgca aagcttcagt gctcgggtcc ctgggacacc ccggccaccc 1080 tcgcctggta gatgtggcat ttccatgctg aggccgcgag tcccgcctga ccccgtcgct 1140 gcctctccag ggcttctctg ggccgcgcct ctgcagactg cgcagccatg ctgcatctgc 1200 tggcgctctt cctgcactgc ctccctctgg cctctgggga ctatgacatc tgcaaatcct 1260 gggtgaccac agatgagggc cccacctggg agttctacgc ctgccagccc aaggtgatgc 1320 gcctgaagga ctacgtcaag gtgaaggtgg agccctcagg catcacatgt ggagaccccc 1380 ctgagaggtt ctgctcccat gagaatccct acctatgcag caacgagtgt gacgcctcca 1440 acccggacct ggcccacccg cccaggctca tgttcgacaa ggaggaggag ggcctggcca 1500 cctactggca gagcatcacc tggagccgct accccagccc gctggaagcc aacatcaccc 1560 tttcgtggaa caagaccgtg gagctgaccg acgacgtggt gatgaccttc gagtacggcc 1620 ggcccacggt catggtcctg gagaagtccc tggacaacgg gcgcacctgg cagccctacc 1680 agttctacgc cgaggactgc atggaggcct tcggtatgtc cgcccgccgg gcccgcgaca 1740 tgtcatcctc cagcgcgcac cgcgtgctct gcaccgagga gtactcgcgc tgggcaggct 1800 ccaagaagga gaagcacgtg cgcttcgagg tgcgggaccg cttcgccatc tttgccggcc 1860 ccgacctgcg caacatggac aacctctaca cgcggctgga gagcgccaag ggcctcaagg 1920 agttcttcac cctcaccgac ctgcgcatgc ggctgctgcg cccggcgctg ggcggcacct 1980 atgtgcagcg ggagaacctc tacaagtact tctacgccat ctccaacatc gaggtcatcg 2040 gcaggtgcaa gtgcaacctg catgccaacc tgtgctccat gcgcgagggc agcctgcagt 2100 gcgagtgcga gcacaacacc accggccccg actgcggcaa gtgcaagaag aatttccgca 2160 cccggtcctg gcgggccggc tcctacctgc cgctgcccca tggctctccc aacgcctgtg 2220 ccgctgcagg ttcctttggc aactgcgaat gctacggtca ctccaaccgc tgcagctaca 2280 ttgacttcct gaatgtggtg acctgcgtca gctgcaagca caacacgcga ggtcagcact 2340 gccagcactg ccggctgggc tactaccgca acggctcggc agagctggat gatgagaacg 2400 tctgcattga gtgtaactgc aaccagatag gctccgtgca cgaccggtgc aacgagaccg 2460 gcttctgcga gtgccgcgag ggcgcggcgg gccccaagtg cgacgactgc ctccccacgc 2520 actactggcg ccagggctgc taccccaacg tgtgcgacga cgaccagctg ctgtgccaga 2580 acggaggcac ctgcctgcag aaccagcgct gcgcctgccc gcgcggctac accggcgtgc 2640 gctgcgagca gccccgctgc gaccccgccg acgatgacgg cggtctggac tgcgaccgcg 2700 cgcccggggc cgccccgcgc cccgccaccc tgctcggctg cctgctgctg ctggggctgg 2760 ccgcccgcct gggccgctga gccccgcccg gaggacgctc cccgcacccg gaggccgggg 2820 gtcccggggt cccggggcgg ggccggcgtc cgaggccggg cggtgagaag ggtgcggccc 2880 gaggtgctcc caggtgctac tcagcagggc cccccgcccg gcccgcgctc ccgcccgcac 2940 tgccctcccc ccgcagcagg ggcgccttgg gactccggtc cccgcgcctg cgatttggtt 3000 tcgtttttct tttgtattat ccgccgccca gttccttttt tgtctttctc tctctctctt 3060 tttttttttt tttttctggc ggtgagccag agggtcggga gaaacgctgc tcgccccaca 3120 ccccgtcctg cctcccacca cacttacaca cacgggactg tggccgacac cccctggcct 3180 gtgccaggct cacgggcggc ggcggacccc gacctccagt tgcctacaat tccagtcgct 3240 gacttggtcc tgttttctat tctttatttt tcctgcaacc caccagaccc caggcctcac 3300 cggaggcccg gtgaccacgg aactcaccgt ctgggggagg aggagagaag gaaggggtgg 3360 ggggcctgga aacttcgttc tgtagagaac tatttttgtt tgtattcact gtcccctgca 3420 agggggacgg ggcgggagca ctggtcaccg cgggggccga tggtggagaa tccgaggagt 3480 aaagagtttg ctcactgctg cctccaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaa 3537 2 530 PRT Human 2 Met Leu His Leu Leu Ala Leu Phe Leu His Cys Leu Pro Leu Ala Ser 1 5 10 15 Gly Asp Tyr Asp Ile Cys Lys Ser Trp Val Thr Thr Asp Glu Gly Pro 20 25 30 Thr Trp Glu Phe Tyr Ala Cys Gln Pro Lys Val Met Arg Leu Lys Asp 35 40 45 Tyr Val Lys Val Lys Val Glu Pro Ser Gly Ile Thr Cys Gly Asp Pro 50 55 60 Pro Glu Arg Phe Cys Ser His Glu Asn Pro Tyr Leu Cys Ser Asn Glu 65 70 75 80 Cys Asp Ala Ser Asn Pro Asp Leu Ala His Pro Pro Arg Leu Met Phe 85 90 95 Asp Lys Glu Glu Glu Gly Leu Ala Thr Tyr Trp Gln Ser Ile Thr Trp 100 105 110 Ser Arg Tyr Pro Ser Pro Leu Glu Ala Asn Ile Thr Leu Ser Trp Asn 115 120 125 Lys Thr Val Glu Leu Thr Asp Asp Val Val Met Thr Phe Glu Tyr Gly 130 135 140 Arg Pro Thr Val Met Val Leu Glu Lys Ser Leu Asp Asn Gly Arg Thr 145 150 155 160 Trp Gln Pro Tyr Gln Phe Tyr Ala Glu Asp Cys Met Glu Ala Phe Gly 165 170 175 Met Ser Ala Arg Arg Ala Arg Asp Met Ser Ser Ser Ser Ala His Arg 180 185 190 Val Leu Cys Thr Glu Glu Tyr Ser Arg Trp Ala Gly Ser Lys Lys Glu 195 200 205 Lys His Val Arg Phe Glu Val Arg Asp Arg Phe Ala Ile Phe Ala Gly 210 215 220 Pro Asp Leu Arg Asn Met Asp Asn Leu Tyr Thr Arg Leu Glu Ser Ala 225 230 235 240 Lys Gly Leu Lys Glu Phe Phe Thr Leu Thr Asp Leu Arg Met Arg Leu 245 250 255 Leu Arg Pro Ala Leu Gly Gly Thr Tyr Val Gln Arg Glu Asn Leu Tyr 260 265 270 Lys Tyr Phe Tyr Ala Ile Ser Asn Ile Glu Val Ile Gly Arg Cys Lys 275 280 285 Cys Asn Leu His Ala Asn Leu Cys Ser Met Arg Glu Gly Ser Leu Gln 290 295 300 Cys Glu Cys Glu His Asn Thr Thr Gly Pro Asp Cys Gly Lys Cys Lys 305 310 315 320 Lys Asn Phe Arg Thr Arg Ser Trp Arg Ala Gly Ser Tyr Leu Pro Leu 325 330 335 Pro His Gly Ser Pro Asn Ala Cys Ala Ala Ala Gly Ser Phe Gly Asn 340 345 350 Cys Glu Cys Tyr Gly His Ser Asn Arg Cys Ser Tyr Ile Asp Phe Leu 355 360 365 Asn Val Val Thr Cys Val Ser Cys Lys His Asn Thr Arg Gly Gln His 370 375 380 Cys Gln His Cys Arg Leu Gly Tyr Tyr Arg Asn Gly Ser Ala Glu Leu 385 390 395 400 Asp Asp Glu Asn Val Cys Ile Glu Cys Asn Cys Asn Gln Ile Gly Ser 405 410 415 Val His Asp Arg Cys Asn Glu Thr Gly Phe Cys Glu Cys Arg Glu Gly 420 425 430 Ala Ala Gly Pro Lys Cys Asp Asp Cys Leu Pro Thr His Tyr Trp Arg 435 440 445 Gln Gly Cys Tyr Pro Asn Val Cys Asp Asp Asp Gln Leu Leu Cys Gln 450 455 460 Asn Gly Gly Thr Cys Leu Gln Asn Gln Arg Cys Ala Cys Pro Arg Gly 465 470 475 480 Tyr Thr Gly Val Arg Cys Glu Gln Pro Arg Cys Asp Pro Ala Asp Asp 485 490 495 Asp Gly Gly Leu Asp Cys Asp Arg Ala Pro Gly Ala Ala Pro Arg Pro 500 505 510 Ala Thr Leu Leu Gly Cys Leu Leu Leu Leu Gly Leu Ala Ala Arg Leu 515 520 525 Gly Arg 530 3 80959 DNA Human misc_feature (1)...(80959) n = A,T,C or G 3 gagttttaat accctggcta tcagcccccc ttggttcctg aggactctta aaagaaaata 60 aagcacattg attctatttg tttctgggag ctgcagtttc ttaataatat caggtgaaga 120 taaattttcc acggagaaaa cgatcctccg ggatgcagct tcttactctg aaaatttccc 180 tgccgactcc tcactctctg cgctcctcct cgttatccgg ggactcctgc ctctcttccc 240 ccttctcttt tttctttttg gcagaacccg cctgcaatat tcgtgtgctg agctcgtaat 300 tccccctgcg atgccagcaa cgcccaattg attgactagt tgtaaacaca tttttcccct 360 ggcagatttt gttgttgtta gggtttttaa aatttattta ttttccaggg aatgcgtggc 420 atttaaacca acaggactgc aattaataga tttgcgagtt gcgccgcgcg cgccgctcgc 480 cccagcctcc cggcctccgg gcctcgctgc ctccccgcgc ccggcggcgt ccagcgccct 540 gcaagccccg agcagccgcg ggtcctgcag ctgaaggaag gttgcagctg cgccctcctt 600 gcaagccgca gcccggcgtc ctggttgtcc cagcagccag gagatcccta cctgttagtg 660 aacagttagg agtcgactgc tggaagaatt aattaggaac gtgctgtgct ctgggcagcg 720 cgagctcggg tagaggcatc caaacctttg ccggcggcgc tattttattt ttactacatt 780 ttctcaggtt gcaaaaatag acaccgggca cgttctttct tagagttttc tagcaaggag 840 cgccttcaag gccaggcagg ctctgtaaca ggttcccctt taaacagcca gaggtgagac 900 ggggaaaatg gtcctggctg ggttctcgtt catctccatc agcagtcctt cacccagaga 960 gaggggcagg ggtcgcccta actcagatga atgagtccca tgcctggagc cctggggccc 1020 tggctggggg ctgctccgag cctgaggtgc tcagggcgct cagggcagca agtgtccgcc 1080 acttcggttt gtcatttttg gcaggagcgt ttttctgtct gggtggagaa tggagtttca 1140 cggaaacaca gttaactctt caggggcctt gcaagtacag gaggtgaaga ggatgtcagg 1200 ggagagccag gtccagactg gacatttggg gtggtttggg aaatcaaatg caatcatcga 1260 agacatatta accagaataa ttaatcatgc aggcactttt ttactgcagt aacctttgcc 1320 ctattggcca atatttttgg ccagaatccc atgctggctg gacttggatt ctccgggtga 1380 cgtatccagt gtctggaaca caccacagta ctgcagtcgt gttatttccc aatgtaacat 1440 tcatgtaact ggtatctatt ttgatataat atattaatta tatctatttt gattttaaat 1500 aattaacaga agcttaaaat agcacagcaa taatcgtaat tgtaacccat ttatagacct 1560 accctctaag aatgatttgc aaaatgctgg ccttgatcag aaaaatctga actcacaaag 1620 cattgttacc tctttggcag tcttcaatat ccctagtttc ttacagttaa aaaaaattaa 1680 atttgccatt tcagattgtg cctatgattg gggggctgtt tctcagtgcc tggctcttca 1740 tggttggcca gcacgtggag cactctgttc atctgtacat ataggtatgg gtccatctgc 1800 acctatagtt acatgctcat ctttgccttt aacaactttg acattctgac ttgacagtca 1860 tggtatttta aagcaaccat taaatcttgg ctcctgggga tgcttttgaa agtctctgac 1920 ccccaagccg gggcacttct gctgaactaa cactcccata aatgagaaaa aaatgcatca 1980 ccttttaaat aacatgcccg atctccaaat gtgcaactct gatattaata aaaataaccc 2040 agttttctcg ggagactttg ctaatgcagc ctcatttttt gcacattttg ccggagagct 2100 tttgttctta tacgtctcta ttctccccct ctttaatttg ttgcaggtgt tgttgctaat 2160 gagctctctc tctctcctcc cctcttacaa tgaaagacaa gtcagacccc aggtacctgg 2220 atggattgag agctgagatc tcagaaactt cataataagt tgccgatggc taccagccaa 2280 ggtcagctgg gccccattag tgccggcccc caccaaagca gaaccaaata gccttctccc 2340 cagtgaacac ctcagtagct tttcattcta gtccagtcac acagctgttg ccaccttaag 2400 ctcatatgaa agaaatctct tttattggtc tgagaaccca agtccagtcc caaagaggga 2460 acatgtttcc agctaacatg cccacctcct gattttattt tatctttaca acgcaggctg 2520 gagggttgtt ttgccgttgt gttgagcacg tcacccatta agagcccttt aaagacctgg 2580 attgattgga aggacaaaaa ttaaaagcaa tctgatccag cctcatgcag gatccctgcg 2640 gattttctcc ttatcccatt tccatccact gtcacaattt gagaatctgc ctgatttgat 2700 cagattcacc tccaggggag gtgtgatacc agggttagga ggacgtgaag ttatgggcaa 2760 ctttctgatc tgtccatcag cagtctgaga aacgctggct ctgaattttc cgtgtcggcc 2820 ttttggaaac aacaagttcc tcgctgtttg caaagcttca gtgctcgggt ccctgggaca 2880 ccccggccac cctcgcctgg tagatgtggc atttccatgc tgaggccgcg agtcccgcct 2940 gaccccgtcg ctgcctctcc agggcttctc tgggccgcgc ctctgcagac tgcgcagcca 3000 tgctgcatct gctggcgctc ttcctgcact gcctccctct ggcctctggg gactatgaca 3060 tctgcaaatc ctgggtgacc acagatgagg gccccacctg ggagttctac gcctgccagc 3120 ccaaggtgat gcgcctgaag gactacgtca aggtgaaggt ggagccctca ggcatcacat 3180 gtggagaccc ccctgagagg ttctgctccc atgtaagtcc acttactgct cttttgtttg 3240 cccaggccaa gtgggaggag gtctggagga gatccttggg gtggacgagc agagctggag 3300 gactgagatg caaggctgac tttcctgcct cttgaccagg tctggaccag acctggacca 3360 ggtctttgtc ccaccttgga aatgtgtcaa aacagaggac accctgagga cactggggtc 3420 atgtgacatt gttctctggg gtaggggcat tctcggccag ctggccacta gttcagttcc 3480 ctcgggaagc ctatagtatt cagctccgca gccttcaggc taagccccac ctcctgtgta 3540 ggaagtcagc attctgggcg agtgagcaag atgctacctg caacatgata ctgtaagctc 3600 cctctgttca tcctttctgt ggtgcaacct cttagcccac tcaatccaat ccagcagacg 3660 gtaccatgaa gctagagcat gccaagcact gagctggccc tttgcatggg gaggtttgac 3720 ggaggctcag aggggattca cgcaggatga agttgggggt taagctggga cagacagtgc 3780 agcttgggtc cccttccact tccattccta catgcaatga tggcagcccc tgggtaagtc 3840 gggggaaggc agacattcag gcgttgtccc ttgcctccct agctagagaa ggaggggtcc 3900 taggggcacg gagtacttca gtactcaagt aatgttaaca gcaacaacaa cagcagagat 3960 ggttgcgtgc gagctgtctg agtgtgtggg ccgagcctga tgccattgcg aggagtcctc 4020 ccctcagcta gccaggtgga ttctgtgttg tataaagcag gagcgtcagg ggagggctct 4080 ggcccagtga cgtctgtggg cttctgttct gtcatctgca aaatgggcac actaagagca 4140 cacactccta gggtcattgt gaggagtttg tggtttaatt aacgtaggta aagtgttcgg 4200 aataggacct ggcacagagt aagtgcacgc agatgttagc cgttgtcatt ctggtcatac 4260 aggtggggta actgaggcag cccaggggtg acgggtaaag gcatctggcc aaggtcacac 4320 tccaggaggt ggcgaagctg tgattccagc ttagagtggc tccaatgtct ctgagctaag 4380 ctgcttccca ctgggcagtg ctccggaggc cgtccctggc agggcagggc agagctgggt 4440 agggcagcca ggctgcagaa gctcacagga ggggcttgat gccatccccc aggcagctgg 4500 tacctctgcg tgtccttgga ggagcctcca ggtctctggg tttgtggtgg ggctgacccg 4560 gtgcccccac ctcagagtcc tgaggacttg atctcatggg ccggctctgc tcacatcaca 4620 gggcagtcag cctgagaagg tagcttctta ctcaggcttg tcagtggtga tgaggctgtc 4680 actgtgggtg gtggctgggc cagggccagc tggggagaga gagagggagg gagagaggga 4740 aggagaaggc ggcacggagc caggagctgg ggctggatag tctgtggcca taactgcccc 4800 ggggaccgca gggccgagca agggggctgg gctctggaag ccaggaggaa ggccaggata 4860 ggggctggta ctcagtccac atctcaaagc cggtgggagg gttctccaca cgctctcggg 4920 cacggtcaac ctctgtctct cgtattagag tctcgactgt attttctctc ttaaatatta 4980 atcactgcct taacgtgctt gggggagcag ctaaatcata attctaggac cagctttggg 5040 tcgagggctt gaggtgggga gatgaccctc agagtcaagt ccgaggccct ctccttgcca 5100 aagctgtcta gggtgtcatt ggccctggac ctctgccctg cccccaccct cagacagaga 5160 acccagtgca gtgggcggct gttctgggga ggtggtcacc cctcccagtc ccagtgccgg 5220 cagagcctca tcccaggcag ccagcctcaa gccctggggt ctagaagagt gctctctccc 5280 atccccatcc cctgctcctc tcctgggcag acaggtgggg aaggcagggg agaaagaaca 5340 gtccctccac aatctcccac atgggcaagt cctcggcgtc tcgccacctg tgtgatggac 5400 ttaaatattt catcatgggc tgccatccag ctctgctttg attacaaatg tgtgtccgat 5460 gaggacgggg aggccgccgt ggcaggtgga cggcagcctt ttgcagggct ggcttttgga 5520 gggctggctt tggagggctg gcttttggag gggtggtttt tggagggggt ggttacttct 5580 agatagatct gggttcaaac cctgatgcca cagtttattg tggcttcccc tgggagggtc 5640 cgggcagtag gatgctctga ggtaggtcct actctaatct catttttggg aatagaaagt 5700 gttgcctaaa tcctgccaac atcactccgt tgagaaggca ggctgggaac tgcctgtagc 5760 caaggcccat gcccacccac caggcggcac agcctcccct ctctccactt ctgacctctc 5820 tgagtttcac tgtcttcctc tgcccagtag aaaccataat gtaggagtgt cacggtgctg 5880 gcgggacggc acagcccggc cgtgctgccg tggtacgtgc ggacacatag taggtactca 5940 gtgtgcaata ctagtcacca gcttatcact gttgtgatta tggcctcggt gattttcctg 6000 gctttgcttc ttccccgggc tcctttgcct ctccccagcc ttggggacgc cacgccttgt 6060 attgctagtc tctggcagca tgtggaagat gcaggctggg ggagcttcct cgcctgcagc 6120 cccagcagct gttgttaacc agccaccagg gggcgcccta atggcggcca gatgcccact 6180 gcccccttag ccttgccatc gcccatgggt ccttgctccc cttcgcccct tcagcggcag 6240 gtgctacgtg tgtcccaaca tccagcccac gggagcgcaa gcccggctgc actccgaggg 6300 tacaggaggg acccaggggc ggacggcctt ttcagatgcg gggtgcagac cctctctctt 6360 tcccaggctt cctgtccttc agcaaggcca cctgagaact gaattgtaaa ttccagcctt 6420 gcaaggaagg ggaggaggct gaaagacaag ataaatgaat aaataaaaac ctattggctc 6480 taaatgcaca atgagaatta atagggatga gctctcaaca gaggattctt gggcaaggac 6540 aaaattgcaa tgagggctgt gggagaagag aggcggcccc cacccacatt cccagggcct 6600 gcccctgagg tcagcccagc aaggctgcag gccgagaagg aggcaggaag ggcgacgggc 6660 aaaggcatct cagcccctca cagggcaact gctgcttgca ggacccttgg agatggggag 6720 ggcgtgactg gcattgggag gtgcccctta gcgctctgca agacacgtct cccgccagcc 6780 acctgtggtc cccgtgagag gaagggggaa acccttcctt tgtgccttgg agacaaaaac 6840 tagccacccg agactcaggg gtgagctgac gagcaggtga gagagagaga gagaactact 6900 gcccaggcag cagggtgcca agggaatcct gccactccca ctcagagcaa tcgcctcagt 6960 gcagcagcgc tgacctcacc ttgatagagg tgcagaatcc cagaccctgc cccacaactg 7020 ccgagccaga ctctgccttt taacaggaag tctctggagc gctggggtgg gggttggtcc 7080 aggatggtgg atgaagcctg ccgttgacga aggggccaga ggtctgtggg tcccatgggg 7140 tctgtgcagg ttaagaggag aggcattgct gaggggagac aggagccaac aggagagcac 7200 tagggggtcc tgggaatgga gggatggagc tgggagccga gattcccaga tgcgggcctt 7260 gcttgccaag gcggggggtc tgtgcttctg agcaggagcc agtggaaggt tccagagaga 7320 ggcagcacta cctcctgaca agagctacag gcctagaatc tgaagccctg agctcacatc 7380 ccagtgttgt cacttggggg ctgggtggtc tgaggtgagt cattcaaatt ctccaagcct 7440 cagtttccct atctgtaaaa ggggtatgat cttcactgcc ttgcccacct caccgacttc 7500 ctcggagagg aaacgcctct cacaacataa cagaaggtgc ttggcagaga ctgtaagttc 7560 ttttctagtg tgaggcttga atattattgt ttatccaatc ttgataagct tgacatttct 7620 acattgacat gggtgaacat tcaaatttca gccatgttgg agtctccagc atacagaggc 7680 accttggctt tggtggacag gaaagccaag ggcaggctgt gaacgtgcat ctttgaacac 7740 acatcttact cagttagaac ctgctttagc ttctctgtgc ctcagtttac ccagctgcag 7800 agcaaatggt tccattcctc ccccaggggg tctgctgggc tgttgaatgc agacagcagg 7860 caggtcctgg agtccttgag ccactcctca ctgtgacatt gaacaccaca tgcagaatca 7920 aggtcacaga cactctgcct cctgccagac cttgaggatc atgaaatgtt tccatccaac 7980 aatgcagagc tgaccggccc gatggctctg gcctccttcc ccctctgtgt ttctggcccc 8040 agcctccctc ctctcgccgt cacaaccctc cagtcggcag atgtttccag gtatgacctc 8100 atgccaggca cagttgtgat gggaaagtga gatgactaga gataaattaa gtgaaaaaca 8160 agagaaaaac actacagaca ttgaagacaa tacccagcta accacaaatg gtgacaccgg 8220 ggcctgatat gataggagct ggggaaggag gagggcgtgc ccctccccat gaactctccg 8280 ggcgctccag ccttggcccg tgctgtctcc tccacccgaa tgcctgcccc ctccttcctt 8340 tcttttcaag gcttccgctt ctacctggat aaccctggct cctttttcaa ggttcaggtt 8400 ggaccctacc tcctcctcca ggaggccttc tctgactcct ttgcccagtg gggtgaggag 8460 gccctcattt ggtcatcatc ctgcttactg actggcctat cagtgaagag ttctggccct 8520 aggaatggag agtttagaat cccgtgctgt gtgatctctg atgtgagacc taacctctct 8580 gaaccttagt ttctcaatgg gagctattaa tagaacgtgc ataggagact gtcatgagca 8640 cggtgcttgg cacatagtag ttgctcactg cgtgctggct gttgggacca attctgtaac 8700 tttagatgtc tgcttttccc ctggactgtg agctcctcaa aggcagggct gtctcgctat 8760 ctttgcatcc ccagcacctc cctctggact tgatcagtgc ccagtaagca tttcctgaat 8820 gaatggatgc atgggaggaa gcatggtgtg atccaggaac gcttctcaga ggaggcagga 8880 tcagggctgt attttttttt tttttttttt ttttttggag tcaaagtctc gctctgtcgc 8940 ccaggctgga gtgcagcggc gcaatctcgg ctcgctgcaa gctctgcctc ctgggttcac 9000 gccattctcc tgcctcagcc tccccagtag ctgggactac aggcacctgc caccacgcca 9060 ggctaatttt ttgtattttt agtagagacg gggtttcact gtgttagcca ggatggtctc 9120 gatctcctga cctcgtgatc cacccacctc agcctcccaa agtgctggga ttacaggagt 9180 gagccactgc acttggccag ggctgagtct tgaaggaaaa actggggttt gggtcaggac 9240 agaggagacc ctggaagccc ctgcttctct ccactgcagt ccctgttctg tgggatttgc 9300 gattggatga agccgggagg tttgcacaac tctgtcctta agtcagttgc aagtgacttc 9360 ggcacctgag ctgcaccagc cgttaaagcc actcagtctc ttgaaatgcc cgaggcaggg 9420 cccagcctag gacaagaata gttctgtgaa atgacatctt gttgcacagt gaagtctccc 9480 tcctgggcag tagacaatga gaagaccgag gcccggggcc cagggagtga gacccttgct 9540 tctgacttcc cttgagggaa tgaggttggg tccagacacc ccgtggaagg caggcagctg 9600 tgtgaaaggg cccagacggg acatctttcc aaagaatgtc agagacttag agacccccag 9660 acctttccgg tttgcgcatc cccaccttcc caggctgtct tcctctatgc ttcctaactc 9720 tgatgtttaa tccatttccc tttttctcat ttactgtggg tataatgaca agctgcctcc 9780 aatcccacct gcgatggggc aggcagtgga cggatggaca gacgaacgga cagacaggca 9840 ggccgcacca tgctgcggat gagacggatg gatggacaga cggacagaca ggcaggagca 9900 ccatgctgcg gatgagatgg atggacggac gaacggagag gcaggcaggt cgaaccatac 9960 tgcggatgag acggacggac ggacagacag gcaggccaca ccatgctgcg gatgagatgg 10020 atggatggac agacggacag acaggcaggc cgcaccatgc tgcggatgag atggacggac 10080 ggacggacag atggacagac aggcaggagc accatgctgc ggatgagatg gatggacaga 10140 cgaacggaca ggcaggcagg tcgaaccatg ctacggatga gacggacgga tggacggaca 10200 ggcaggcagg ccacaccatg ctgcggatga gatggacaga cggacagaac ggacagatag 10260 gcaggccgca ccatgctgcg gatgagatgg acagacggac agacggacag acaggcaggc 10320 cacaccatgc tgcggatgag atggacagac ggacagacgg acagataggc aggccgcacc 10380 atgctgcgga tgagatggac agacggacag ataggcaggc cgcaccatgc tgcggatgag 10440 acggacggac ggacaggcag gtcgaaccat gctgcagatt agacggacag atggacggac 10500 ggacagacag gcaggccgca ccatgctgcg gatgagacgg acggagacag acggacagac 10560 agcaggtcga accatgctgc agattagacg gacagatgga cggacggaca gacaggcagg 10620 ccgcaccatg ctgtggatga gatggatgga tggacagacg gacagacagg caggccgcac 10680 catgctgcgg atgagaactt gggcttctgg agggaggaga tggggcccgg gggcatcccg 10740 cacttctggg atgtgggact tgggataagt cccttgtgac cctgagcctt ggttttctca 10800 tctgaaactg ggcatggcgc tggacacaac ctcgaaggac gtgtgtacaa ataagacgag 10860 accaggcgtg tgatgacctc agctgggagc cagcacaaaa ggaatgctca aaaaaagggc 10920 cgggtgcacg gtggctcaag cctgtaatcc cagctctgtg agaggctgag gtgggcggat 10980 cacctgaggt caggagttca agaacagcct ggccaacatg gggaaacccc gtctctacta 11040 aaaatacaaa aattagccgg gtgtggtggc gcgcgcctgt aatcccagct acttgggagt 11100 ctgaggcaag agaatcactt gaacctggga ggtggggttt gtagtgaact gagatcgtcc 11160 cactgcactc cagcctgggc gacagagcaa gactctgtct caaaaaaaaa aaagtgtatt 11220 tttattttta tcctttttaa ttctagaatt tagcttgagg gacagaagag gaccccatag 11280 gccaaaccca cagccagagg cacaggctgt gggctcagaa gtgggtcttg caggatggga 11340 agggtcagga gagtgaggat gtgggcagaa ggaatggttc gtgcagagac gcagggaagg 11400 gggccaggtg attcgagggg aaagtgcgtg ggtgacagag aggagacagt ccactccccc 11460 tgcccacctc atccaagccc ctgtaggtct gttactgtgc atctgaccgg tgaatattct 11520 gagacttctc agagcccact gagtgtagga gctggggttc agccttcctg tgtctggctc 11580 ctgaccgctc gctagggtta ggaaggatta ggccacgggc tctgaaggag caagaggggc 11640 aggagggcaa ttgaggggca attgagagga acccagaaca tggaagccct gtgccgtggg 11700 gctggtccag agctcaccag gctggaccac gtggttgctg agccatggcc cctgaccggg 11760 gctgacctgg ccagagtccc tgtggccagc actgatgcag ggctccttcc tagaggggcc 11820 gggccatgag gaacgggaga aacggcagat gatgcgggaa ccggtctgtt cggctttggt 11880 ttgcaggatc cgatttgttt ttcatcagca gcagatttgc ttaagtatat gaaaatgtgt 11940 ttctaattcc ccgagcacac accaactgct ggcgggggag ggagcagtgc ataggagcag 12000 agtgaatgcc accgggagtc agagtgctag gccctggctg ctgagagagc gagaatacgc 12060 ccccagcctc agtttcccca actgagcagc cggggaagat ttggctagat taaccagttc 12120 attcaatgtt ccctgctgat tgccaggtac attctgggag tttagggaaa tccagattgg 12180 tcagagacaa aaccacacaa aacagtggac tccagtgcag acagaggggt cctagatgta 12240 taccccgggc tcagcatagc aataatcatt ttaaaaaaga ttttaaaaca tttttaaaac 12300 tcaggtgaag ttcacataac ataaaattaa ccagttaaac aacgttttgg tgggtgcagt 12360 ggctcacacc tataacccca gcactttggg aggccgaggc aggaggatca cttgaggcca 12420 agagtttgag accagcctgg gcaatgtagt gagaccccat ctctcaaaaa aaaaaaagtc 12480 ttattgtgtc taacataaaa cttgcctttt aaactatttt acaatataca attcagtaca 12540 ttcacaatgt tgtgcaacca gcatctctac ttagtcccaa cacgtttcca tcgccccaat 12600 agaaaaccct gcacccgtta gttactcccc atctccttcc cctgcccctg aaaaccacgc 12660 gtctactttt tgtctccatg aatttagcta tgctagacat ttcatacgaa tggaatcaga 12720 caatatgagg ctctttgtga tggccttcct tcactggcaa aatgtttcca aggtttgtcc 12780 acattgtcgc atgactcagt gcttcattcc tgtttatggc tgcataatat gccatcctgt 12840 ggacacacca tattttgtgt atccgtttcc taactgatgg acatttgagc tgcttctgct 12900 ttctggctat taggagtgat actgctgtgg acatttgggt ctcagttttt gcatgtgtgt 12960 atgtcttcat ttctcttggc tgtctaccta aaagtggagt ttctgggtca caaggtaatt 13020 ctatgtgtaa ctttttgggg agccaccaaa ctgttttcta caggtgctgc acctcttacg 13080 ttcccaccag caatgtacga gaatgccagt ttctccgaat ccttgtcaac acttgttatt 13140 ttctggtttt gttttgtctt attaggatga gcctagtggg tgtggggcag tatcccatta 13200 tggtcttgat ttgcatttcc ccgatagcta atgatgtcag tgtgcttctt agtcattttt 13260 ttgtttttgt ttttgttgtg tgttgttttg agacagagtc tcattctgtc acctgggctg 13320 gagtgcagtg ttgcgatctt ggctcactgc aaccttcacc tcctgggttc aaatcattcc 13380 tgcctcagct cccaagtagc tgggattaca ggtacacacc accacaccca cctaattttt 13440 gtgtttttag tagagacagg gtttcaccat gttgcccagg ctggtctcga actcctggcc 13500 tcaagcgatc tgcccgcctg ggcctcccga agtgctggga ccacaggcgt gagccaccac 13560 gcccagccta ttttaaattt aatgaactcc aatgtgtgta tttttttctt ttgttgcttg 13620 tgcttttggt gtcatatcta agaaaccact gctaaatcca aggtcagcag tatttacccc 13680 catattttct tctaagactt ttatagtttt agctcttata tctaggtctt tgatccattt 13740 tgagttaatt tttgtatctg gtgtaaggga aaaggtctat ctttattctt ttgcatgtgg 13800 agatccagtt tccccaacac tatttgttga agagcctatt cttcccccac taaatgttct 13860 tggcaacctt gtcgaaaatc aattgagcat aatctatgca cttacttctg gactctcaaa 13920 tctctgggtt tttttgtttg tttgtttgtt tgttttggag tcagagtctt gctctgtcac 13980 ccaggctgga gtgcagtggt gcgatctcag ctcactgcaa cctccccctc ccgggttcaa 14040 gcgattctcc tgcctcagcc tcccaagcag ctgggattac aggcactagc cagcacgccc 14100 agctaatttt tgtattttta gtagagatgg ggtttcacta tttggccagg ctgatctcga 14160 actcctggac tcaagtgatc tgcccacctc ggcctcccaa agtgctggga ttacaggcgt 14220 gagccacagc gcctggcctc aaatctattc ctctgaagca tcaagcattc tatgtgcact 14280 acttcatgaa accctcctgg atattctgca ctgtagaaac gattactctc ctgttgtgcc 14340 cattttatag atgaggaaac tgagactcca aaactgagtg aagtcaaggc tcaaactcag 14400 atcccagtca tttgatgact aggccacagt gaggcctgag gaggggaaaa atcccaatgg 14460 ttaccctccc cttcccctcc ccaccctcat tttcttctcc ctctttcagg ctgggatgtg 14520 gacttggatt ctcagagcag ggtccttgga aggagatgct gtgacttctc tctggcctcc 14580 aaatacctcc tcagcctcca gtccacctcc gtccctctcc cacgcagcca ggcactgttc 14640 tgtcctcttc cttgtcccac agtcagtgct tgcatgtagc aggtacttaa taaatgctga 14700 agataattat ccatcatttc aaatagagac acacaactta gaaggcatgc tgggattgtc 14760 taaggccaga aaaaccccaa tgtcgataag catgttacag tgaaattgac tgcgcccagg 14820 aaaggggacc ccagaagcag gtggctggtg tccccctacc ctgccccagg ccccgagttc 14880 cccaatccac cactaggaag tcctgggctc ctgtgaagac aatataaaac cactgattag 14940 gccaagtgtg gtggctcaca cctgtaaatc ctagcactct gggaggctga ggcgggcgga 15000 ttgtctgagc tcaggagttt gaaaccagcc agggtgacat ggtgaaaccc catctctact 15060 aaaaatacaa aaaaaaaaaa aaaaaaaatt agctgggtgt ggtggtgcac acctgtagtc 15120 ccagctactc gggagactga ggcagaagaa tttcttgaac ctgggaggcg gaggcagagg 15180 ttgcagtgag ccgagactgt gccactgcac tccagcctgc acaacagagt gagactcggt 15240 ctcaaaaaaa aaaaaaaaaa aaaaactact gatgaggcac atccccccct ctcatttcct 15300 atgaaggaga aactgaggcc cagagggttg gagtgacttc cttgagcccc ccatgaggag 15360 cttcagaccc tggaggctcc accccaggcc aagggctctc ccagaggtag actggagcca 15420 tgaggacagg ggccctcccc aaccaggtct ctgtccatct acacgtgccc tggatctgac 15480 ttcacgtgat ggcatctggt gggggacaca ggatgcctgc ccggatgcca cctgcagcca 15540 gtgggggccg gagctgcctc ttcagggtca gtgagggtga tacatctact tcccagcctg 15600 cttaggtgag ctcccgccta tgtgtcacta ctggtgactg gcatggctca gagccagatc 15660 ttgggggccc tgaggggatc aagagcgtcc cctaagccca cctgccagct gcggtcttct 15720 ctgtggtggc agcatcacag aaagtggaca gaaagagtgc tctgtgccag gagggcaagg 15780 ccgggtagga tggtggctgg aatgctggcg atcgcagcaa tgccggcgat catggtgctg 15840 ggttttggtg gtgtgctgga cgcctgggag cctcatgagt gagagactgg ggcacacgtg 15900 cttccgtagt gccatgcacc ggtggcaatt cagagaaaga cgctgtgcaa agcaccccat 15960 gtgtgcagct ttttgccctc tcgtaacagg acggagccag gtcagagtgc agatgaggag 16020 aggaaggtgc agggaggtgg agatgctgac ccaagtttgc acagccaaaa ctaggatcgg 16080 tctccagggc ctccgtcact gtcctgtcct gccttctgtc acacaggagt tcgaatggtc 16140 gttctgaaat tgagagctag cggggctggg atctcactgg gcggccacag aggggtcccc 16200 tgacctcttg gggtctcgtt ggcaggaggg aattgtattg gaatatccag gtgtgtggat 16260 ccctgtgaat ctaaccctgg agtgttccag aactgcccac cctgtggaaa gggactcagg 16320 cctgtcttca aggacctggc atccttctgt cccagggcag tttgtcttgg gtctctcagg 16380 gaccgtttgg gcctcttcag cccctcattc cacttccctc ctgctgccca agtcattcgt 16440 ccacttgact ccaagagtcg gctggggaaa taaaaggaaa tgaaacacga ccaggcattt 16500 tcccttggcc gaagcagaag tctgctgtcg ggcaaaaggt gaagaagaga ccaatgagag 16560 atgagcccac ggtgctcctg ccctccgcca aggcaggcca tcctctgctg ccagcctgca 16620 acagggcagt gtccttctgg gaggtgtccc tccctctggg ggatcaagag atggccaaaa 16680 gcaggtggca gcaagtggag aaggctgttc atccagaacg caccttgtct ctgcccctgt 16740 ccccacccag gcaacatcca aaacctttgc ccacagttcc ggggctggca ccgtcctggg 16800 gctcagctcc tagggacggg gctcccccag gcactggctg ccaggaactg ggtggccccg 16860 ggcaagtctc ttcccatttc ggggtataga cttcctgcct gtaaaatgag ggggtctgca 16920 ggtcaacctc agagtcccac tgtaccccca gattctgctt cagggagacg gagagagaga 16980 gaaagagaaa gaacgataga gagatgcaat aacctcccag catccaggaa gacccagagg 17040 ggagaaatgc agggaaccta cccagaaaac cctggagcgg gagcttctca cttttaatgg 17100 tcatggcccc acttgagaat ccatggtgct cttcctagaa ccacgcatgt gcacacgtgt 17160 gtgcaaacac tgggctcatg cacaggcaca cacacacaca tataaggttg caaacacttt 17220 cagggacttc ccagatttct ctgagtccat ccgtggtcac tttcggtcaa tcatctggcc 17280 tgagcaggtt ctgccttctg ggggctcttc taccctcagg gaaatcaggg tttggttccc 17340 tgtaattgtc tggtccaatt gtctgaggac tttctctttt ttttgagaca gggtctcact 17400 ctgtcaccca ggctggagtg cagtgaagca gtcttggctc actgcagcct cgacctcctg 17460 ggctccagtg atcctcccac ctcagcctcc tgagcacctg ggatcacagg catgcaccac 17520 catgcctggc taatttttgt atttttgtag agatggggtt ttgccatgtt gcccaggctg 17580 gtcttaaact cctgggctca ctttcttttt tttttttttt tgagacggag tcttgctctg 17640 tcacccaggc tggagggcag tggcatgatc ttggctcact gcaacctcca cctcccaagt 17700 tcaagcaatc ctccttcctc agcctcccaa gtagctggga ttacaggcac ctgccaccat 17760 gcctggctaa tttttgtatt tttagtagag acaaagtttc accatgttgg ccaggctgat 17820 ctcctgacct taagtgatcc gcccacctca gcctcccaaa gtgtcgggat tacaggcgtg 17880 agccactgtg cctggccata gccagacttt cttgattcta tatccttctc ctcagagcag 17940 aaacatcgag catttgttga gtgcctcatg tataccaagc ccttaaccta agctatagct 18000 cattgaactc tcacagaagt cttaaggtag agcttgtatt tagatccgtt ttgaatatga 18060 ggaatctcag gttcagagaa tttaagccac ttgccgaagg ccacacagct tctaagtaga 18120 ggaggctggc acctccagcc tgggccgccc ggcccggcat ccaggttcct aaacaggctg 18180 ctcagctgac acgagtcgct ctggatctca gaaagcgcct gatagacgga ggcggctgtc 18240 atctgtgtgt gtgtgtgcgt gcgtgcagcc atgtgtgctg gtgagcatac tgtccctgtc 18300 agcctctcct cccccagcac accccggcag cccagagaag ggagggcccg gaggagtgac 18360 ggtgttcccc accccctgcc ctttgagaca caatggagtc cgctaatcca gttacttgat 18420 aattcactta tttcatgtct atttggcagc gagcgtgctc ccacgcacca gctctgggga 18480 aggcgagatg gctttgcctg gaggaacctg attgtttttc tggggaagga gtgggggaaa 18540 aaattgcacc caacaatgga caataatggg cctaaaaata gagggtggag ggtgcagggg 18600 gtggaggagt gtgctgtctg ccaagggagg gctccaggcc tgtctgcttg gcacggggca 18660 gccctaccct cctgcccagt tcccctcccc tgcactgggt tggccgcctc tcagcctaga 18720 ggaggggcac tggaaggagg aggcccaagt gggtgggggg ctgggtggcc ttccttgctg 18780 tctctgcccg ctccaaaatg gaaaattgtc ccacccaggg ggtcctggag gcagcagcca 18840 cgaccttggg tggacgctgc gcctcatcag ccctgactag ccgtgatgcc caggaccttc 18900 ccccaagggg ctcaggcatc agctgagaac tgcagccttg ggtacagagt acgggttgtc 18960 tcccagcagg aaagggaggt ttcaggtttt gtggctcttt tccatctccc aacacttggg 19020 gcagtcttct cgaaggcctc aagcccagcg ggcagctatg accccaccag gagcggagcg 19080 ggcagggacc aggctgccct ctaagccact cggctggctc tcagccgggg tgcacactgg 19140 acttgcctgg gagcttttca ttccccccct gccgcagctg ccccccagac cagcttcagc 19200 agcctctctg ggcggcccag caggaggagg cattaaacct ccccaggtgg tcccagtgca 19260 cagccaagtt tgagaagcac cgattgaaac ctctcccagg cctgccctgg agcccttcca 19320 gcctgaagca tcttgtcgtc ttaaaactga aagaccagga ggaagagaat tccatggcct 19380 gcctcggctc tctcggagcc tctctcacat ctgagctgca ggtgctccat cctccttctg 19440 gcttcctggg tgccgagggg tgccagctct ccaggcttgg gagagggcca cttaagccct 19500 cacactttgt tcccaggctc ttcacctgtc ttcctggaag gagggggccg gccagcatta 19560 gggctgtcac gggcgctgct taatgtcaag ctgcccatct ggctcctggc ctccctttgg 19620 ccttctctcc tgcgctcccc accaagctcc tggctcagca gcgtgcatgc gttaacccat 19680 tgcccccctg cagtgttttg tgtgtccagc ctggcccttt gctcagtcga cctagagcac 19740 catcctccca gactagtcga gtgtccctcc acctgtcctg agtccagatg aaatcccacc 19800 tcccccagga agccttctga ctgccccagc ccgtcacctc cagggcttgt catctgtgcc 19860 actcatgggg accaggacac aggtgacttc tctggtggac acagcagaac ggtcaacatt 19920 cccaaaaggg agcaaattgc ccgagtcacc agaagtgtga ccttgagcaa gcatctggct 19980 caggggctct tggcttcccc acctgtaggt aaaataacag gaacagtgtc atcgtgtggg 20040 ggcccttccc tggaccacct ggaccagcct ctcaaacctg gccacacatc tgagtcacct 20100 gctgagggtt ttggttagtt ggttggttaa ttactcgatt ggttagtttg ttggtttgtt 20160 tgttagcttt caatttggag tagaatttct gaccttaggg cccaggaatg ttgccacacc 20220 cctcccgtcc ccaggtattg tcatgttttc atgggtggcc aaatctaaga gctgcttctc 20280 tggggcacga aggatgttca caaatagttg atgaataagt gaatgaataa atcaatgaaa 20340 cttaccagcc cagcctcact actcgcaccc acccccaacg accagccagg gttcatccac 20400 agaggggtgt acctgtccag gtgtccccag gtgtgggcag acccagtaac tttactcttt 20460 catcggcccc accgcctctt aactcctcag agaccagcag gaagaaaccc tcggaggtcg 20520 cagcttctgg ctgttctcag gggcaggccc cgtccatcgg gtgctgtgtc tactcctaag 20580 acctggttct gagtatggaa cacctggaga gggaaggggc cgaggagggg gagtcactcg 20640 gctgtgtcag gctccgcccc tgccttcctg aagcacacag tggggagggg acacacccgt 20700 cattaaccga agaagccact ggggaaaact gtgacccagt gctcccttgg gactgggggg 20760 cagtggccag gggtgttttc cctgaggaaa agaaatttaa gcagacacct gccaaaggct 20820 ggagggagag ctgtagacag aagatggctc aacctgaaag ctccgcgggg tggagggggc 20880 atccaaaggg cgggagagac tggccagtag aaaacgaggc cagaagccgg acatggtggc 20940 tcacgcctgt aatcccagca ctttgggagg ccgaggcggg tggatcacct gaggtcagga 21000 gttcgagacc agcctgacca acatggggaa acccagtctc tactaaaaat acaaaattag 21060 ccaggtgtgg aggcacatcc ggtaatccca gctacttggg aggctgaggt aggagaatca 21120 cttgaacccg ggaggccgag gttgcagtga gccaagatcg taccagtgca ctccagcctg 21180 gacaacaaga gcgaaactct gtctcaaaga aaacaaggct ggaaagacaa gggagagagg 21240 cagagctggt ggcagagcca ggcccagggt ttggacttaa gaaggggaag gcgctggggc 21300 tctgaggagg agctggagac aaagggaagg gtgtctggct gcaggctgag aatgggctgg 21360 gggtggggag gctagagggg tcggtggagg ccccaaccaa ggcggggcag gggagaacag 21420 agtgagcctt taggagaaac cactgctggg gaccaggctt cactctcagc ccatccggaa 21480 acctctttca gctgatgctt cccccgaccc ccttccccac cctgggcctc tgttggaagc 21540 tggctgaggc cctgttgatc agcaagaaag cccagggcag ctctcagaga agaggagagg 21600 gggcccagaa aaggccccca ggatctgggg aggggatccg aggagaggca gctaccaagc 21660 gccccagcca ggggggcctg tccctcaccc caccccggca ctgaaaccct cacagccact 21720 tttttcctcc ctccgtgata aaatattcat ggcggcagag tgggccctct ttgggaaggc 21780 tgcctgggtc tagcttatgc tctgcacaag cttttaaaga gcagggcgct gttcctactc 21840 tctaagcatt ttctaagtcc tgaatcaata atgcactttc ctgggcttct ccggatgtag 21900 ccctcttcct ctcggtgcct ttcccccgcc cgccccctta tctttctttc ccttttcttc 21960 tctcccgttc tttcatcctt ccatctctcc tttcatttac tttttaaaaa agtatgaaag 22020 tgttgagctg tttgggtggc cagtgaagcc ctgagtaggg agtgggcagg aagggaggcg 22080 ccagactgag cccctgtgtg tgcagggagg aggaggagga gtgggaggag gaggaggagt 22140 gggaggagga ggaggagtgg gaggaggagg aggagggaaa ggaggaggag cagcagcggc 22200 tgagcgctcc cgctggccct gctagggaag tgtttgagga tcactgagct cctggtgtgg 22260 ggaaggagga gggcttagcc tcacccggcc tccctctctc ctttttctaa tcaattagaa 22320 agtgtttaca gcatagccag agaaaaatag ggaacctggg accaagaaaa aatgcaaagc 22380 accggccaaa tttcagcccc acactcgaag gagggagcag tggggtttca cctatctgcc 22440 ttctgtggta atgaaacccc tgtcgctaga ggtatgcaag agaaggggag ccttaccctg 22500 tctgagacag acgcccatgt gtctggtcca ttctgtcagt cgcctgtggg gtgccccagg 22560 gatgcacggg cactcttcaa ctgggataga atttcctgcc ccaaacattc ctggaaatct 22620 ggctgtggga agaatccaca tatgcccagg gcaaagcaga atgtgtcctt taagaaaaca 22680 ataatacatt tttaagttcc tggagagatt aacccttgtc tagccagagc catggcaatg 22740 cctccccgcc caccacactc tggtggttcg gctgacggag gagatcagtc attcaggggt 22800 ctgcggtcct gatgagcagt gggtgcccac accaggcctg gcatttcatc cttgctttct 22860 gaccttggct tcccagttga ccctctcccg ggcagctcgt ccatcagggc agcccaatgc 22920 cctcaggtcc tccgaaagga tctcagggtg ttctgtgggg gcaacccgaa ttggtgtaag 22980 aagactaagc agtcgatctg ctggaacagc atccccaaag cggagcgaag cccgcggatg 23040 cccaccgcct ctcccccagg cagcgtccta cctggataga actgcctgga gccactgcag 23100 agggtcctcg ctcagttagg gaatgtttgt catataccgc tgtgtgcaaa cagctgttgg 23160 gagtgtggcg caaaggtggg taaggcccct gctctcccag agttcacact cacagaaggt 23220 tctggaagga ggaacactgt gggcagggtt gaaaggccta aagtgctccc tttcctccca 23280 aataatgcgg ggtgaggggc ggtgaggaga gccgctctga gcaaccaagg aactgagatg 23340 cattttctgg gtctcctttt gagccgaggc aggttcgaga ggcagccaga gactctgggt 23400 tcaaggtgga cctgtgccca ggccatgccc actgtggccc ccctggggga ggagcagggg 23460 cggtcgccgt ggctttggga ggctcattgc tgggacaagc gagtccctgg ggaggcagcg 23520 cttggaggct cgcttgcctg cccctgcctg agtaattgct tggagctggg aggaaaattg 23580 ctccaaccag aaaacaaaac agaaaagccg ccttggccag ctgcagctcc agccctaaaa 23640 tgccaggttg gtttacgctg attcacgagc ggggagggtg accttgctgt ctgttgtcca 23700 gggcctgtgc acgaagagaa tctggaaagg gaaggagaga gacacctgca cgctggggaa 23760 ggaattagca gcacagagag caagagggac agcgatcaat gaaaccatag aaggagaatg 23820 agaaacacac acacagagag cgagagggag caagagagag agagagagag agagagggac 23880 agaaaacgag agggagggag ggagggagag ctcagagagt tagagaccgt cagggccgct 23940 agaattagaa tcagctctga acagaatctc cgtttccgct ttgttaataa tttattccct 24000 ctgcaacttt tcttaccaat aaataggaag taatctgtta aggagaattc ccctagcacc 24060 ccggctttct ccctggagtc aggggaggag gatgtgtctc tgtgcccttc ctccctagca 24120 gcatgggggc ctgaggaaca cgcagaactt cagactttag gatgtcaggg tcagaggcgg 24180 acagcccact cctgcccggt cattttgtga acggggaaac caaggcacag atagggcaag 24240 gccctggcca aggtcacaca tggtgttagg ggcagtcccc tgagtcctaa ttccatggcc 24300 ccacgggtca gggcacctat tgatttatgc acctgcccaa gccatagggt ttcccccgaa 24360 atggcagagg ccacatccaa ggaggagggt ggggctagct cggctgcctt tccttgcctt 24420 cccccacgat tgcttccccc gtgctcgagt cctggccctc tacctgggca cccacaccca 24480 gggcctctcc tgggcagcct ccagccttcc accttgtatg cggcagcagc ctcccgtcct 24540 ggtgaggctg aggggctgag gatgagaagg gttccgttgg caaatcagca acagcagtca 24600 agagacgtgc cgcctgcctc cccgtggaac ccgagtctgc gggagcacag tgcggcccag 24660 gcaacagcgt cctttccctt ttgggtgaag ggcaccattt cccaatttgt ctcagggccc 24720 agctcagtgg gccatcccct ggcttcttat cccacctcag ctgctgccga gccgcatgac 24780 cctgcgacat tgctcagcct ctctgagtct cggtttcctg aggatcgcac tctccaggat 24840 ccctgggagc gtgggaggtg gggttggggc acacagggcg cccagcacag ggccgaggtg 24900 gaagacatgc tccctaacgg cggggcctgc tgtttgctga agcaccaggc cagacagtgg 24960 ccatgaatgt gctcccagca tccatcaccc atgagctggc accaccgagg cacttgccat 25020 ggtgcacctg gcatcattcc tatgacaacc ctgtgaagcc agtgctagta acctcattga 25080 gcgttcattc attctccgaa gatttcccga gtccctgagg agggccgggg gctggggctg 25140 gagtggggac aggatcagat gtggtcgctg cccgcatgaa gcctcccctc caacagagaa 25200 gctgaggctc tcgggcagga gaaagatctt ttcctcaccc attctatgtt agtggctgag 25260 ggcccatcat aacagacaaa ttaataccac caaagcatac cagtggattt aatataagtt 25320 ttatgtgaaa aaggctttaa gcctttcttt tttttttttt tttttttttt ttttagacag 25380 ggtctcactc tgtcactcag gctggagtgc agtggcacag ttacggctca ctacagcctc 25440 gacctcctgg gcccaaggga tcttcctatc tcagccaccc aagtagctgg gaccactggt 25500 gtgtgccacc atgcccggct agttttcttt tttgtttttt gaggtttttt tctgtagaga 25560 tggcatctcc ctgtgttgcc tggcctcatg ggagctttca taaggaatga agacccaaaa 25620 cattggtgaa catctatttt gtatgctagg tttaatggag aaatagtcat ggagaagtac 25680 gattggctta aaaaaaagta tcatctcctg gtgataaact ggcgggaatt ttgcaagacc 25740 tgtgtgtcca ggtccctctc tgtgaccctg catctttgga gatgagaatg ttccttcctc 25800 cgggcattgg gagggcacct ctcgaatgag cctcatgtcc tgcttcaggg aagaagggca 25860 ggggaaggtc aaagagtaac cttccgcttc tgtggttttc tcaaatccct tcagcttaaa 25920 aaaaattatt tttttgagac ggagtctcac tctgtcaccc aggctggagt gcagtggtgt 25980 gatctcagct cactgcaacc tctgcctccc aggttcaaat gnnnnnnnnn nnnnnnnnnn 26040 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 26100 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ngggaggccg 26160 aggcgggcgg ctcatgaggt caggagatcg agaccatcct ggctaacacg gtgaaacccc 26220 gtctctacta aaaatacaaa aacttagctg ggcgtggtgg cgggcacctg taatcccagc 26280 tacttgggag gctgaggcag gagaatggtg tgaacccggg aggcagagct tgcagtgacc 26340 cgagatagcg ccactgcact ccagactggg cgaaagagag agactccatc tcaaaaaaaa 26400 aaaaaaaaaa aaaaaaaaaa agaaggtttt agggtagcat gtcctgggct tcattgggct 26460 caaggaaatt gggggactcg cccaagcctg tggagctggg ggagctgctg aggaagtgag 26520 ccagtgcatc cttccacaaa ccacagagcc ctgcccggga caccctggcg atttcatccc 26580 aactctgaga tttcatccca gcgcaggctt gggtgcaagg ccagctgcat gacgttgtct 26640 gttcttcttc ctgagacttg gtgaccattc cagtgaccgc ccctccacgg cctccttagt 26700 caggggcctg gaagttcaaa tggctgggct tcccacaggc acatttacct ccattcttgc 26760 taacagttca ctttcccatt caattatgtt ttttgcctgc agcttgccta tgatgtttac 26820 aacctggcct ctgactttga ctgtaccctt tgcacagaaa ataacataaa aggaaaagca 26880 tttaagtgcc catgacgagg cttgaaaagc atggcatgaa atggtttctc catagaatat 26940 ttcatgccag gagctcaggc ttggcatctg tgtaggaggc tcctcctcac ccggttctct 27000 ggtgctatgg gcctggctgg ctgccttccc ttccctctgc ccaccctcct ttgacttcta 27060 gccacactgc ctgacctttc aggtgacttg cctatgtgtg tccagagaga taggaaagct 27120 gtagacatga tgggcttggt ttccccaaga ttcctcaagg ttgggtcccg tggagtccag 27180 gggatgggta agtgatgtgc ggccatgggt acttagtgtc ttatctgaga cgtggagctg 27240 actgtagcac ctgcctcctg tgggttgctg agagggtgca gggaggagcg gctgtgaagt 27300 gcccaaccca gcccgggcac agggctggca ctcagtgaat gttacaatca tcacactctt 27360 ctgagtcagc cgttcccggg acagtccacg ccatgaagtt ccagggtttc tcatgcacaa 27420 gcctggtggt ctcagcctca tcccttcctc ctgtggaagg ttgctgggag tggagtgtcc 27480 ctgagttaat acgaagctgc tgtttcaaaa taatcgctcc cgtttggaga cacttcctag 27540 ggattctagg taatgtgaga cacagaccat ctcacatggc aatcaataag aaaatagaga 27600 ctcagagaag tcaagtgact ttgtcaaggt cacagagcct caaaggagag agctgagagg 27660 gaactcaggg ctttcagacg ccagggccca aaactgtatg gaaaatgggt atgttaactg 27720 catctttctt tttttttttc ttttagacag agtcttgctc tgtcgcccag gctggagtgc 27780 tggagtgcag tggcgcgatc tcggctcact gcaagctcca cctcctgggt tcacgccatt 27840 ctcctgcctc agcttcctga gtagctggga ctacaggcgc ccgccgctac acccggctaa 27900 ttttttgtat tttttagtag agacggggtt tcactgtgtt agccaggatg gtctcgatct 27960 ccttacctca tatccacccg cctcagcctc ccagagtgct tggattacgg gcgtgagcca 28020 ccgcgcccgg ccattaccgc atctttctag agaaaatccc aagactcttt ttaaaaatca 28080 gcggtatgat ttttgttgtt gttttaattt tcatgaaata tttaaagagg cagctactac 28140 ttctgatact atcaaagggc ggctttggag ccatgctgaa aggctagagg tgtgcctaac 28200 agtctctccc tatattaggc cactttgttc tgactgctgt ttttgtgatt agttgatctg 28260 ctgtcctgga gatgggtgga aacgcgcaga cccagaggag gctggcaaac cttcaccccc 28320 actcagagga gacactccca gtctcagccc cacccccatg acattatcag ctgtcagatg 28380 ctgactgggg actggggtgg ggggactggg gtaaactggt cttctaatac cccggtgggt 28440 ccccagaatt cccccagtga agaatagaag gtccaggtgc aatggctcac gcctgtaatc 28500 ccagcacttt gggaggccga ggtgggcgga tcacctgagg tcaggagttc gagaccagcc 28560 ttgccaacat ggtgaaaccc tgtctctact aaaaatacaa aaattagcca ggcgtggtgg 28620 cgcacgcctg tagtcccagc tacctgggag actgaggcag gagtatcgct tgaacccagg 28680 aagtggaggt tgcagtgagc cgagattgtg ccactgcatt ccagcctggg ccatggagca 28740 agattctgtc tcaaaaaaca aaacaaaaca aaacaagaat agaaggaaag tgagaggaag 28800 caatactgtg tttgtagagg aaaaggaagg tcaggtcagc gccaacagtg cctttgctgg 28860 gatgctccac actcctgacc agctcagtgg aattctgaga ccttggggag caaaatcaga 28920 gggggacaag gagaaagaca gaaagagaaa gagggagaga gaaaattgtg ttggccgcgg 28980 ctcgggattt atttattgta cttgctgttg actgagctcg ctccacagca ggcgaggggc 29040 ctgtaaacac acaggctgat tcattagttt ctgaccatct gcttcccggg ccggggcggg 29100 ggccggagtg ccccataggt tggagcagcc agcttagagc ccccatctcc agccagagcc 29160 agctgtgtca gtcttcccag tgacagacag gccgggtgca actgggggct ttgagggata 29220 ccctgtcccc cgccacaatg cccccacccc atagaaccca tcaggggcct gggcagggca 29280 gggctaagta aggcaggaag atgaagagag accagggaaa aggtgaagtg tgggtggctc 29340 agcagttggg gatgacggga atactatcaa cactcaatag gagatatgtc aatatcactg 29400 tcattttatt aatagcttat taatatgatg ataataataa taagtataat tgagtgagtg 29460 gttactgagg tccaggccca atatgcaggc ctcactacac tgtccccaat aagcacatta 29520 acaactctat gatggatgat gagagaactg ggttcaaaga ttgattcaag tcaggagggc 29580 ctcctggagg aggcacatgt gggagggctc tgaaaaccag gaggacagac agtggccaaa 29640 ggagcacagg ctctgaggtg ggaggggacg aagtggcctg ggaaatggca cagcttcagt 29700 gctgggttga taagagcttt ctgggtaggt gacgcagtgt gacgccactt ggtgccagcg 29760 tactgagaaa ccaggctggt ggaggagacc ccagagacat cctctgggga aataggatga 29820 aaaactccca attcgtctct acccctctga gccattcctc ccggcctgtt ccctctttgc 29880 tcacctggca tgaggcttgt cttagtcagc tccggccacc ataacaaagt agcacacgag 29940 acccaggtgg cttaaacaac aaaaatgtct ttccttgttc tggaggctga aagtccaaga 30000 tgaagttgtt ggcaggtttg gtttctggag aggcctctct ccctggcttg gagccagccg 30060 ccttctcact gtgccttcaa acggcctttt ctctgtgcac atgggcccca gcgtctcatc 30120 cggcagccaa acttcttctt cttccaaggc caccagtcag attggactag ggccaacctg 30180 agggtcccat ttaacctcaa tcacctcttg aaagagaatc tgtctccaaa tacagtccca 30240 ttctcagata ctagggttag ggcttcaaca cagaaatctg ggggacacca ttcagcccct 30300 aggaagtccc caggggcagc agaagcagca ctgggacttc aggaagggag tgatggctgg 30360 gctgggggaa ggggggcatg tgcctgggtg ccagagccca ggtgcaagtt cttggagcat 30420 atgcccatca ctcctcctcc cgagcggcac agacagagcc cattctgcat ccaggctcac 30480 agcacccttc ccggctgctg gctccctcac gggtcaagcc tgcctcctcc agcccagcac 30540 ctgctaccca ctcaggccat tgggccatcc ccacagcctc tcagtccctc accattccag 30600 gcaacagcac aggacagggt gtgtcttgcc cagagtcacc cggccagtga gtgaggaagc 30660 tgggaacccc cccgccccat gtccctctgc tgtcctggca tggtgggctt gccagtggtg 30720 tggatatctc tgatgataac agcagactcc tcctcagagg tgccatctgc tctcgagaag 30780 gctggggcca gtcctaccct ggcccgggcc tcagtccccc catctgctta aggagatatt 30840 ggactctatg gtgagctcct gccaccctga ggttgcatgg gggcctgagg acagagctat 30900 tttggtcaaa gagggatttg tggaacctgc ctcaatgaac cgagggtcag ccctgccacc 30960 gaggagcccc aggcagccag gggacctgtc cttcacccta gaggatagaa gcccaaaggc 31020 tgcggctgct gcagtggcac ctggtggggg ccgcggggct gtggctcagc ccctcagaag 31080 gcggtgggcc ccatttcccc catgggggcc aaacagctca tttgagagtg agaggtttta 31140 acttagatcc aagccatttt gtgtctgagc aaaccagaca cctgaaacat gcatcagaaa 31200 gggccacaag tggtccggag cactgggtgg ttgttagtga cagtgttcgt ttttttcttt 31260 ctttctcttt ctttctttct ttcattcatt aatagacttt atattttaaa gcagttttag 31320 atttacagaa aattgagcag atagtacaga aagtacctaa aaccccatgc caccctcccc 31380 cacccaccat ctttccctgc ctattatcca catcttgcat tagtggggga tatttgaggt 31440 tttgggggat ttctcttttt tttgttttcg tttttgtttt tgttttttga gacaaagtct 31500 cgctctgtcg cccaggctgg agcgcagtgg cgtgatctcg gcttactgca agctcctcct 31560 cccgggttca tgccattctc ctgcctcagc ctcccgagta gctgggacta caggcgccca 31620 ccaccacgcc tggctatttt tttttttttt tttttttttg tatttttagt agagacgggg 31680 tttcactgtg ttagccagga tggtgttgat ctcctgacct cgtgatccac ccgcctcggc 31740 ctcccaaagt gctgggatta caggcgtgag ccaccgcgcc tggcctttgt tttggggaat 31800 ttctttagag acagggtctc cctctgtgat ccaggctaca gtgcagtggt gctgcatagc 31860 tcactgcagc ctcaaactcc tgggctcaag caatctccag ccccagcctc ccaagtagct 31920 aggaccacag gtgtgcacca ctatgcccag ctaattttta aatttttttt tgtagataca 31980 gggtcttgct gtgttgccta ggctgatctt gaactcctgg cctcaagtga tcctcccact 32040 tctgcccccc gagtagctgg gactagaggt gcatgccacc acaccacacc cagtttattt 32100 tttattgttt gtagagacag ggtctctctg tgttgcctgg gccgatctca aactcctggg 32160 ctcaagtgac cctcctgcct cggcctcccg gagtgttgga attccaggtg tgagccacca 32220 tattagtcat gtctgatgaa ccattgttga tacattatta ttaactaaag tccataattt 32280 acatgagagt tcacttactg tgttgtacag gtctatgggt ttttttgttt gttttgtttt 32340 gtttttgttt gtttttgttt ttgtttgata cggagtttca ctcttgttgc ccaggctgga 32400 gtgcaatggc acgatctcgg ctcactgcaa cctacgcctc cagggttcaa gtgattctct 32460 tgcctcagcc tccccagtaa ctgggattac aggcatgcac caccacgccc gggtaatttt 32520 tttgtatttt tagtagagac ggggtttctc catgttggtc aggcttgtct tgaactcctg 32580 acctcaggtg atctgcccgc ctcagcctcc caaagtgctg gattacaggt gtgagccacc 32640 gcgcccagcc tgggtctatg ggttttgact cattcataat ggcatgcatc caccactgca 32700 gtattatatg gcatagcctc actgtcctaa aaatgccctg tgctcggcct agtcatccct 32760 ctgaccctgg ggaccactac attagtgaca ttttcagatc cctctggcct gtttccatca 32820 gtgacacttc tcacaccaaa tgtatgggtt ttccacacca acaacctagt ctccagctct 32880 ctggacacca ctgggtgtcc gatgattccg ttcaattgta acactgccca gagctggcgt 32940 cagaaccctc aggtgaaggg ctcagtcgca ccacactgcc cccacctctg acgcaattgc 33000 aagttcctgc ctcccgtact tctgtccaat tggctgtaaa ttgggggttc ccacgacccc 33060 tccctcaggt ttgatagttt gctagaacag ctcacggaac tcagaaaggc attttcccta 33120 catttacctg tttatcaagt tcaggaacag ccagatagaa gagactcaca gagtaaggga 33180 tcggggagag acccagagct tccaggccct ctttgagcac ctcaatgtgt tcaccaatcc 33240 taagggtaca ggtaaaaagg ctcaggggcc aggcgcagtg gctcacgtct gcaatcccag 33300 cactttggga gggcaagcca ggtggatcaa cggaggtcag agttcgagac cagcctggcc 33360 aacatggcga aaccctgtct ctactaaaaa cacaaaaatt agccgggcgt ggtggtgcat 33420 gcctgtaatc ccagctactt gggaggctga ggcaggagaa tcgctggaac ctgggaggtg 33480 gaggttgctg tgagccgaga tcgccccact gcactccatc ctgggaaaca tagcaagact 33540 ccatctcaat aaaaaaataa aattaaaatt aaaaaataaa aggctcagga aggtgactca 33600 gctaaggaga tatttagaga gtcgagaatg tgaatgggaa tttttgaggc ggacagagtg 33660 gaagggcaca tgaaggagac agaatgccat ctgcaaaggc tcagaggtac aaccaggcag 33720 gggcaggagg acagctgtcc cggggaggcc caggcacagt gtcaccaggt gtgggagggc 33780 aggttggggt tggtatatta cagagtcagg actctgtatt ccaggcaacg gggagccatg 33840 gagggcttca aagcagggga ctaacaccca gccttcttgg ttgtctgtat ttagagcaag 33900 gacaagtatg cattttttct ttggaagcca tgggattgca cacctctgca cgcattgagg 33960 aaatgggcac aaatctccca gctgtgtctg ggcaccggag cacaggccct gtagccacag 34020 agcaggtttc tcggttcgca ggcaggggct aggccgcgca gaggcttccc aggccatccc 34080 aagcatgcag cacccaccct tcccttctcc tctccccgct gcaggagaat ccctacctat 34140 gcagcaacga gtgtgacgcc tccaacccgg acctggccca cccgcccagg ctcatgttcg 34200 acaaggagga ggagggcctg gccacctact ggcagagcat cacctggagc cgctacccca 34260 gcccgctgga agccaacatc accctttcgt ggaacaagac cgtggagctg accgacgacg 34320 tggtgatgac cttcgagtac ggccggccca cggtcatggt cctggagaag tccctggaca 34380 acgggcgcac ctggcagccc taccagttct acgccgagga ctgcatggag gccttcggta 34440 tgtccgcccg ccgggcccgc gacatgtcat cctccagcgc gcaccgcgtg ctctgcaccg 34500 aggagtactc gcgctgggca ggctccaaga aggagaagca cgtgcgcttc gaggtgcggg 34560 accgcttcgc catctttgcc ggccccgacc tgcgcaacat ggacaacctc tacacgcggc 34620 tggagagcgc caagggcctc aaggagtttt tcaccctcac cgacctgcgc atgcggctgc 34680 tgcgcccggc gctgggcggc acctatgtgc agcgggagaa cctctacaag tacttctacg 34740 ccatctccaa catcgaggtc atcggcaggt aaggccgggg gaagccctgg atgtcacctg 34800 caacctggga tgctatctgt tacctgggac gttattggat acctgggatg ttacctggta 34860 tgtggaacat gaccaggttc ttgggatgtt acctggttcc ctgggcgtta cctggtatgt 34920 gatacatcgt tacctggttc cccgggggtt acctggtatg tgatacatcg ttacctggtt 34980 ccctgggggt tacctggtat gtgacacatc ccctggttct tgggatgtta cctggtacct 35040 gggacatgac ctggttcttg ggatgttatc tggtacctgg gacatgacct ggttcttgga 35100 atgttacctg gtacctggga cactatctac ttcttgagat gttacttggt ttccaggagg 35160 ttacctagca cctgggacat tacctggttc tcaggacatt acctgatatt acatcatagg 35220 gactgcctag gatggctggg gctgcacaga cccaatgcct gagcttttcc acggaagaag 35280 gtgcacatgt cggaggaagg aagtgcatgt gttggaggtg tggagggcag gagtggagcc 35340 tgtctgggca gagctgggct aactcctggt gctgactgtg agaagtgctc tgaggctgtc 35400 cactgactca gtgaatgggc tctcatgttc aggggtttcc gagaccgccc tcaggctcca 35460 tgattcacta gaaaatctca cagaactcag caaagctgct atattcacag ttatggttta 35520 ttacaatgaa ggatacagat taaaatcagc aacaggaaaa ggtgcacagg gctgggtcca 35580 ggagatacca ggtgcaagct tctcattgtc ctctcccagt ggggttgtgc aggcagcact 35640 tgattctccc agcagtgaca tgggacaatg cttgtgaact atcaccaggc agggatgctt 35700 actgaagcct cagtgttcag agtttttact gggagatgat ggtataggca ttgctgatga 35760 tctggctggc ctttggctcc aatccctcca gaggtcgagc tgatactaca tggcccaagg 35820 cataggctct ctgatgtggc ccaagacccg caggcaaaca tggacactct tcctagacag 35880 gacactccaa cggcttatgg attagaggtc acctagcaga aaccaggccg gagtcagatc 35940 tttctttgga atgtgcaggg tgtggacaac ccaggcctgc tgtggcagct ctttcttgcc 36000 cagctctgga gaggaatgtg ttttgaggaa actttgagga aggcaaaaga ctgtcatagg 36060 agatgaaagc agcctttacc tcccaaaaac tgtttagact gtggatgatt aaatggttct 36120 gtgttgtcct gggtcatttg tacttttggc agataatatg ccagtctgtg ggggcaatgc 36180 catctaccct gggccatctg tagaatgggg atggtaacaa gcataagtct cttgctggat 36240 tgtggtgagg gttaaatgag ttaaagttga tgaagcacac cgaacagtgc ctggcacata 36300 atacgcacta aaaaaaagtg tttaataaaa aaattggaca aaataatgga gtgagagggc 36360 tggggcgggc tgagggagga gagagttgag acccaagggt gctggggcag tccgggccag 36420 gagcctggct taggcaggtg caggcagggg ctgcacctgg ggagcccagc tgggatgatc 36480 actgtgggca tctctccact gcaggctttc aacgtccacc caaatctgta attcctgaca 36540 agtggaaaaa gtgatttgcc gtatggcagg tagagcataa tcctgttttt gtaaaatata 36600 taatatgcct tgtatatcat ttctgcgtct tgaacagaca ttggctgtaa gtgtgtacag 36660 gaccgggaaa aacatcatgg gttggggaga aaggctggaa gcccgtttgc cagccatgtg 36720 ctgtggtgat gcctgtgccg tgaggctggg caggccgctg tggtgctgct gtttccagct 36780 tgtatttgca ttttgtttca ctttgacgct gtgtgtggat tccaggtggg caaaggcaaa 36840 ggcaggtcgt tcatgaagct ggagtcagct tcaagtctgg cagatgggag tgaagcaggt 36900 gcagacaggg gcccgtggtt ctgacacccg tgatctctaa cccacctcca attgggacag 36960 gatattcaaa atcaggaatg ttctggaaac caccccatat ataggcactg ttgtggaact 37020 ggtgtccaga ctttcagccc ctgggcatct ccgtgacctc tgccctcggg atgcaattgt 37080 ctggttgtta ctagacacct gccaatccct gcagtcccac tgggcttagc agctcagggc 37140 tgggaaccag ctccccaggc cctgcaggct cctggcttgt cttctgacct tggactgctc 37200 agggaaaccc tcatcttcag gcaactgttc aaggaccctg ccttaccttt cataaggtgg 37260 ctcatgtggg gccctcatgt ctgggccagc tgtaggatcc agactgggac tgtgatgctc 37320 agggcctggt ggtgcccctt caaccccagc agggtgacct ggggttcaaa ccctgcctct 37380 ctgcatcctg ccttgatttc ccatctgtga caagaggcct gaggctgcct ggagcccatg 37440 tctccctgga ggtggttccg cttggcaccc agcctctgcg ggcggcgggg aggagccgag 37500 gtggtggcga gagtgtacaa tcaattcaga gagagagtaa acactcttca ggcggcagct 37560 tggcttgtcg ttgaactcgg ttgggttaga cggttcagcg aaggactgag gttacctccc 37620 cttttccctc ttcagttccg ctgggaaagt ccagccatgc tgagaagcca gagacacagg 37680 actggtggca aagggggatg tgggacccga agttcctgag tgggcaccag ggacccctgg 37740 gggttcccag gctctgggat tttacaccga tcctgttctg gggattccct cagaatttcg 37800 tgactgccat gttgcccagt ggctccgctg tggcccacta acaagaacag caaacgttta 37860 tcgagcattt gctacgggct catttgctat tgagcgctgt tattaacggc ttcatgtgta 37920 ttttcttgtt taatcaatag ccgtttaatt ccccaatggt tattgaatgg ctcagatccc 37980 acaagccaaa gacacggcac tgagcaagcc agacctgatc cccaacccct ggagcgctcc 38040 ccgcgggggc agcgctcccc cagcctcatg ttttcagatg aagaagccaa ggactctgag 38100 gtcagagaat agaaggagat tgcacagcgc cactacatgg cagacagcta acatctagac 38160 acaagcatgt ccaggctcaa gacagactca gccaccgagc tgtccctagc cctggcccgg 38220 tggctgcctc atttctggtt ccagctctga cttgagccca cctggagctc aggtagcctg 38280 tatgatggag cgatcccacg ggactcccct ttgaattgaa ggttctttga tgggtggtgg 38340 ctccctgctc tgccactcaa gtcagtgatt tccagctcca agggggaccc caatggcagg 38400 cagcaatgta ggcaggaggg ggaggacaga ggcacctggc tgcagaggag gagctggagc 38460 agctgcagca gctgcagcca gcccagggcc ctgggaagga gggactggta caaatggtga 38520 gggggacaag aggtggggac agactgagct gcagccccac agggggcagg tgggctgccg 38580 gtggctctga gagaagcaca ggcacccgca agtcccagcc acgccccctc cctgcctccc 38640 gcggagcctg ctccacgtgc ccattcctgg aaggcaggca gggggtggga gctattttct 38700 ccttccacac atggggaaac tcaggtgcgg agcctggaga gtggctggct tcagactgtg 38760 cagcaaatct ggggcagaat ctggatttga ggaggaatga gatcatccct ttatggtgct 38820 tggagcggga ggggcttccg gcccccaccc tccacacaac cattaagaga agcggggccc 38880 aaacctgacc cagcatctca caggagaacc atttaagaca gggttcccca gccccaccac 38940 tgagagcttt gggaccggga ggcttggggt gaggtccaga aggctgtgtc tttgcaaagc 39000 tcctcaagtg agctggaaag gtggaagctg ctgcatccat ggagatggat gactgtaacc 39060 tgttggaacc tcagttttct catctgcaaa atggagaaat agtaatgact tcagctgcct 39120 gttgtgagga gtcgatgaaa tgctatattc aaagagctta tcccagtgtc tcattcctct 39180 ggttagacgg tgggagaggg aagtggggga ggcttggggt cagggctgcc tagatatgag 39240 gccattcctg cacccacccc aggtactaga aggagtgtgg aagcatgcct ctgggttcac 39300 aggggttgca atcccaaatg tctgcagagg ctggaaacac aacttacgtg gaagccaggc 39360 atggtggtgt gcgcctgtag tcctagctac ttgggaggct gaggcagaag gattatttga 39420 gcctgggagg ttgaggctgc agtgagttat gatggtacca cagcactcca gcctgggtga 39480 cagagagaga tcctgtctct aaaaaaataa taataataaa ttcaaatgaa taataaaaat 39540 aatgagaaga agataatgta catgggtacc tatggtacca gcggaagcga tagggaaggg 39600 tgtggcctgg ggagaaatgg agacagcagg cgcctcacaa gacagtggac caaacattcc 39660 agatcttctg cggttacaaa ggaaggtgca cagaagtatc tatgtaaagt ctcttgcttt 39720 caaaaatatt ggcacctact tcaaaaagtt gtttaaactc tgtgcaagga aaacaaaata 39780 cccctgcagc ccagggcagc tcacgagctg ccagggagca cccctgctct gaaatgctca 39840 gtgtcctcct gcagccgtgg tagcagctgc attcgatggg cccaaggcag ggccaacaca 39900 ctggagccag ggcaggggca agatagcaaa acagcccagc cagctctgcc cactccagac 39960 ctgggagtca gagggaaggg ggcatcatcc cacgcaagtt cctctgccca gaaaacccag 40020 gaagctccag gaaggcagcc cagcgggtcc tttgccagca ggaacaggaa aggaggaatg 40080 agttccccat tcctggaggt attcaagccc agtgggtggt gtttgtggga gatgatgaag 40140 ggaggtcctt tgcaccaaat taaggtcttg tgtgcccatt ctgttcaaaa ggaataaatg 40200 tggattaagg gaacaggaaa ggcaggtacc atttattggg aacccatggg ttacgtgcca 40260 ggcattgcat cctcaccccc tttctgccca ggagcaggct gaagtccttg agcgagagga 40320 aacccgtgag ttccaagagg ctgagctggg cctggacggg cagatctgag ctccagactg 40380 gccaagcccg gctcctgcag acccagcttc cccagaccct gtgggggtct agctgctcta 40440 tgtccctggg cctcccccaa cctgtttttt cctcaacacc ctcccctctt tcttgccttc 40500 ttgttttctt ccataaacgt cctgtcccta ttgatcgccc cgtaactgga gatggacgga 40560 caccggacta gaatagaaac agcagaggga agaaaaccat ggagggtggg caggtgggcg 40620 cggggagggg agtgcagaga caggcgattt cagccaccct attcctgtac ccaccctccc 40680 tgcatctctt tctcagctgc tctacaggaa aaacaggggc aagaagggaa ttctgtgatg 40740 ttattctgcc tgcactgact ccttgaaact ctgggaaggc agagacaact ccctcagcaa 40800 tattaactgt cattcactga gaattcccat agcccaggta gcatcccgag tcctttatgt 40860 gcatttcctc attaagtcct atcctgtgag gatcattgtc cccatgacac agatgaggaa 40920 actgaggcca ggaggttgag atatagatgg aagggctggg tgtggtggct cgtgcctgta 40980 atcctagcac tttgggaggc tgacgcagga ggatctcttg agtccaggag ttcaagacca 41040 gcctgggcaa tatagtgaga cccccatctc aatgaaaaca aaatagatgg aggtacccat 41100 gaggatggct attattggaa aagcaaaaaa taacaagtgt tggcaaggat gtggaaaaat 41160 cggaaccttc atgcattgct ggtgggaaca aaaacggtgc agccacaggg gagaacagta 41220 tggtggctcc tgaacaagtt acatgtagat ttagcaattc cgctcctagg tatagaccca 41280 acagaactga aagaagggac ttgaacagat acttgtacac ccatgtttat agcagcttta 41340 ttcagagtag tcaaaaggta gaaacaacac aactgttcat caacaaatga agacataaaa 41400 tgtgacccat ccatataatg gaatatgatt cagccttaaa aaggagggag aacctgacac 41460 acgctgcgac acagatgaac cctgaggaca tgatgctaag tgaaataagc cagacacaaa 41520 aggacaagta ccatatgatt ctgcttaccc gacgtcccca gagtcgtcaa attcatagag 41580 acagaaagta gaatggtggc tgccaggggc tgggggaagg cggaatgggg gttagtattt 41640 aatggagaca gcttcagttt gcgatgattt aaagttctgg agagggatgg taacggtgct 41700 tgcacagcac tgtggatgtg ctaatgccac cagactgtac acttaacaat ggtaaggtgg 41760 ctgggcgcgg tggctcatgc ctgtaatctc agcactttgg gaggccgagg cgggcggatc 41820 acttgaggtc aggagctcaa gaccagcctg gccaacatgg caaaacccca tctctactaa 41880 aaatacaaaa attacctagg tgtgggagcg ggtgcctgta atcccaccta cttgggaagc 41940 cgagacagga gaatcacttg aaccagggaa gtggaggttg cagtgaactg agatcgcacc 42000 actgcactcc agcctgggca acagagagag actccatctc aaaagaaaaa aacatggtaa 42060 ggtgataaat atatacgtat attttagcac actaaaaaat gaaggaaata gatgggtggg 42120 tggtctccat gtcagactgt ccaggtgcaa attctggatt aggtgtgacc ctgggcaagt 42180 tgtctaacct gtctttgcct ccttcccacc tccacaaaat ggagacaatc accctggagt 42240 ttaagtgaga ccatccagag agaggagcca caactgtcag ggttacagag aaagaacagc 42300 agatcacaga gggcctggag gttcttctac tggggcctat gggctcttag gagcgcaaag 42360 ggtgggtttc aatcatccat ggactccctg aaatatatgc taagtgttgt gtgtgtgcag 42420 tcagttggtg agagccccta gtttttgttc cattctcaaa gggggtccat gatcccaaaa 42480 tatttggaga gtccctggaa aggcagcttt gtgttctgct tttcattttt taaacccaac 42540 tcttggccgg gcgtggtggc tcacgcctgt aatcccaaca ctttgggagg ccgaggcagg 42600 tccatcacct gaggtcagga gttcaagacc agcctgacca acatggtaaa accctgtctc 42660 tactaaagat acaaaattta tccaggcgtg gtggcgtgca cctgtaatcc cagctactcg 42720 ggaggctgag gcaggagaat cacttgaacc cagaaggcgg aggttgcagt gagccgagat 42780 cgtgccgttg cactccagcc tgggtgacag agcaagactc cgtctcaaaa aaataaataa 42840 ataaataaaa taaacccaac tctttgggga cacccagctc tttggggaca gacattttgt 42900 taagtacagt tcacacacct tcaactgcat ctcccaggcc ccctgagcta ctgcttccca 42960 ccaaaaagcg ggcatgcacg attccagacc acatcagcct ccactgagaa gtgccggtgt 43020 tgggaagggg ccagactatg ctgaagagtt ggggggtggt ggggtccact gccaaggcag 43080 gtggttgacc cctggacctg cggtctcctc tggtctttgg ctctgctcca ctgctgggtg 43140 gggcggagag ggcaggaggg gcatctcggc cttggccagg gtcacaggag gcttggggag 43200 ccctgcaggt gcttgggaga gagtcacgca cagcaacgcc ttcccagcag cactaggcag 43260 aatcggggtt ccctcttctc ttgcctaaga aggcatttcc tctgcgagct ttctcgccat 43320 catattaatt cactcaacag atgttttttc tcagaccttg cagggatgaa ttaacacata 43380 tttctaatgg gcactgcctt ggtttcttgg agcctccata acaaagtacc actaactggg 43440 tggaggtcag gagtctgaaa tcagggtgca gctggcttcg ctgtggaacc tgcagagggg 43500 aatctgtccc ataccctccg ccctccgctc gctcctggtg gggccggcag cctctggcgt 43560 tcctgggctt gcagctgcgt cactccagtc tctgccttgt cttgcggctg tccgctccct 43620 gagcatctgt cttacacgct gtctccccgt gtctcttcct acagggacac caatcacatc 43680 ggataagggc ccgccctcct gcagcatgac ctcagcttaa cttacatcct catccacatc 43740 cacaaaaccc catttccatg taaggtcaca ttcataggca ctgggggtca ggatgtcaac 43800 atatcttttc gggagacacg atttggccca cagcaggcac ctatgacatg ctggacacaa 43860 gcagggtgcc agggtccaag agcatggagg ggctgacgct cccgtagtgg gagagcagaa 43920 atcaacaaac ccagtacccc caagtgccca caggtgcacg gtgagaaaga aaccagggca 43980 aggccaggca cggtggctca cgcctgtaac cccagcactt tgggaggctg aggctggcgg 44040 attgcttgag cgcaggagtt caagaccagc ttgggccaca tggtgaaacc ccatcacgac 44100 aaaaaataca aaaattagcc aggcatggtg gtgtgcgcct gtggtctcag atacctggga 44160 ggctgaggtg ggaggattgc ttgagcccag gaagtcaagc ctgcagtgag ttatgactgt 44220 gctactgcac tccagcctgg gcaacagagc gagaccctat ctcaaaaccc agggcaatat 44280 gggagtggag ctgggaacca acctgagacc tggacccagg ggtcagggaa ggccctccag 44340 ggaggggggc tttgaaggag aaacctgaag ggggaacggg ggcacggcat ttgtggcagg 44400 gggacagcag gcaggacagg tgcagtgcct tctaaggact caatgtgatg tggctgtggt 44460 gggtgagtaa gattccaaag aagagcaggc agggccagat cacgccagcc ctgcagcccc 44520 gggaggaagt tggttttggt tgaagtttgg taggagggct acaggcaggg gagaggtgtg 44580 atctgatttc cggtgtttgg aaatctgagt tgggggtggc ggtgctggag gcctgcagga 44640 gaccgggcgg gccctaccaa gactgacagc agcctggccg ggttctggca gggacagggg 44700 ctgtgatgtg ggccgcctgg aggtggtctt tggtggcagt gttgctgagt agctgatggg 44760 agcaggcggt gggaggcatc atggaggact cccaggcatc tggctttgag acactgggtg 44820 gatggaaatt ttgccttgtc aaatggggac agaggtgagg ggattttctg gaggggaatt 44880 tttttttaat ttcttaattt tttattttta tattttcata cagcaaagtg gaccttttgg 44940 gggtacaatt ctaggaattt tagcacgtgg atagagtcat gcaaccacca ccacagcctg 45000 ggcccacaac agcccgtctc tccaagaact cccgtcccga gacccctgga agcccccatc 45060 ctgctccctg aaaatctgct gtaagtggag tcgtgcggca ggtggctttt tcaaggggtc 45120 tccttcgttc tcactgtgcc tctgaggctt atggcgtggc cgcctgcgtg gctcgggctc 45180 ctcactcctg agtaggactg tgccgtgtgc actgcacacc gtggtctgtt tacccattct 45240 ccgtggaaga acgtttcggt ggctcccagt ctggggcgat tatgagtaga gctgctataa 45300 acattcgtgg aaaggttttt gggtgaacat aagttttcgc ttctcttggg taaacaccca 45360 ggtgtggacg gctgggtcgt ctggtgagcg tgtttaactc tatgagaaac tgccaggccg 45420 tcttccagcg cggctgtgca ctggaggaag cctgacttct attttggacc tgttggttgt 45480 gagcgttttg gaggcatccg gagcatttgg gcctctgagt gtgaagcgca ggcgagactg 45540 ggcgcgggga gtcctgagct ccgcggtgac gatgacgccc gccgtggggg cgtgcgagac 45600 ttccgagagg agagccgggg agccgggcgg gctgcagccc tgagatcaga gacaggggga 45660 atctggcagg gcggtgcccc aaagccacgc gggagcggtt cctgcagggc agcggccacc 45720 tgtgtccatg ctgcggcggg tccaagtgga ggaggccagc gtgggcccat ggacctggga 45780 agatggaggt cacagtagac gcacccagag cagagcccgg gagtccggga tgaaggccgt 45840 cgtggggtgg tttcaggggt gaatgccaac acttttaaaa gagtgaaata ggggtaaaaa 45900 agagggggtg taggcaagct tttgaaaacg ttttgctcgg aaggggagca gagagatggg 45960 gtgtgagctg ctgggggaat ggggagggga gagggctctt cctgaaagcg ggaggcgccg 46020 cagcgttggc gttgggatgg gaagaatcca ccaggactga agatagctgt ggggagggcg 46080 ggagggacgc tggggacagg agccgaggaa gtgatcgggg tgggcggaga gctgacagga 46140 cagagggccc accagcatgt gtaaggagga aaggctgact gatttcatat ttaggtcaga 46200 aaccctgctt ctaacacctt ctagagactc catgtccatc ttgacaaccc agggtggccc 46260 accctggtgg ctcacagaag tccctttgtc ctgagtaaag agtggcacat cacggtgcca 46320 gcgagcagcc tgcctgagat tccagctctt tccatttgct cttttctggc aagtctcttc 46380 catttctcca ggcctcagtt tccccacctg taaaatggga tcccgctctt gtaaagattg 46440 tctgagactt gcccgctcaa gtcccaatac tcaggaggtg cctgaggaag gggagccatt 46500 gatcccttga aggagtcggt attttgtcac ctgaacacac agaccatgtt cctccgtcac 46560 tcgcctgggg ctgagtggaa ttccttggct ttatctccag ctctgtcctc tgtcccttca 46620 tcagtcaaca gtcatgcagg aatgagaagc tcagttcata gtaggtatag ccaaaggtac 46680 tttggaggag agtgctgctg ccaacagcgg acgggggact gagccccacc cagttctgcc 46740 tgggccactc cctctgggtc tgtggccacg acacccggca ggctcctgtc cccccgaccc 46800 cagctctgtg gcttgctggg cctcaccagc tgcgattggg caggacagat ggggttggag 46860 aggggaagtt gagtggggag aggacaggcc acatccaggc tcatcctcag gccttgttct 46920 gcccctgggc tgggctgcct ccctccacat ctcagcagag ggagcgtggg gtgggtcatt 46980 gtagaggatc cctggccctt catcccatgt gaagcctgtt ttagactcac agatgctccc 47040 ttagatgtac ccgccaagtc acacacacac gcagccattc actcatctgt aacatgcccc 47100 tgactcacac ataaacacac acctgcccca cccacacatg tgaatccgct tccagaagca 47160 cccagtcata gacacatcac actccacatg gctgccttgc acccctgctc acagacgcgg 47220 acccacaggg tgagcggagg cctccgcagc agcccggggt tcaccagagg ccttggcttg 47280 actgccctgg gctcagggct tctctgtgct tctcccccat gttgaggcac ccacttcatg 47340 cttgggttcc tggaggcctc tttccactct gtgggacaaa gccccctctg ggcttctaac 47400 catccctcca tcccactctc agcctgaact aggtcccaag gtggaccccc tatcagcagc 47460 cttgccccct agaagagagg tgcaggctgg cgtcaggatt tggtttcggg acatgactgg 47520 cctccctccc tcccttcagt cttgcccttt ctgtagtttt ttgtccctaa acacaaaccc 47580 agtcacttct ctgcacaata tctctagtgg tcttctactg accttagact caagtctgtg 47640 ctctgtgacc acagactttc cctctcacct ccttctgtag cctgggctct gagactccca 47700 agatcagcca ccccaaaggc tgggtctctc gggctggcct aggggctagt ccttctgcct 47760 ggaacatgac ctagccctcc ccagccttcc tgtctggcaa actcctcacc cctcaggact 47820 tggctcagag agcacctctc tggagctcct gaaggctgga gacctgtgca accagcccct 47880 cggtcccctt ctccagcctt ggcggcttgc gacaattcca cagccttgcc atagctacca 47940 tagctatgca cgtacacgtc tgacacccgc ccccataggc tctgagctcc aagggagcag 48000 ggatggggtc tggcttgttc tcaccttagc accagcaccc agaaccaggt aggcgtgctg 48060 tatatgtgtg gaattcattc attcattcag tcagtcagtc attcatttat tcattcatga 48120 acaaatgaac ttacatgaac aaagaagtct tactatctgg aactctttcc agagaagaaa 48180 gagactggaa tataggcgct aggaggcaga gaggcaggac cagctgggct tgctagcacc 48240 cacccttgtc gcctcccacc cttccaccat cacaccctgc tccttctcct gttttccttg 48300 tgtgagaaat gggcctctct gggctaccac ctgggcctgg tccttccctc gggggtgttg 48360 ggccttcctg caggggaaga agcaaccttg ctgaagtcag ctaggctgct taggctgggg 48420 gtgccttcgc aggccctggt catacccacc gtgtcacccc taagccgcac acctcaagcc 48480 tcccagcacc cgcccgtcag cctctgtgtt gtgtgcaagg aagctgcctc tggctttgta 48540 atgggtaata ggatttatca atagactgag gaggtgaggt atgttaaagc acttaataga 48600 aaagggcttc gcacagaagc ccaaatttga tttagccaat gaactcaatt gccggcctga 48660 ttgcattcca ggaggcgcag cagccagcat ttgtccatgt taccctggaa aagccaggct 48720 gcgccaggcg accaacccag accacccaga cctcccctct gcccccacgg ctctgttgtt 48780 ggttcctcgc tttctcagga tctcaggttt gaatggcagt cctttgaccc aaacagtccc 48840 aagttctcca gcatccaaca gcctccttcc ctctagtgcc caaggcttcc ccatcccatg 48900 aattagctag aagtgcagtt tgctaccatg ttcctttcac catgatcctc aaatccgtgt 48960 gtcccctggt cacttgtcac ctcttactca agctggcctc tgcaggcttc cctcctgacc 49020 atttgtttct tctctggctg ctgcccatct ccccacactg cttgcctgag ccaaggacac 49080 atctctccca accccccaaa gaagaccaag atccccaggc cacagtgttt catgacgtct 49140 tgactcaggc ctgggcatag cagatgggaa ttaccatgta gaaaagaagg acttgaggcc 49200 gggcacaatg gctcatgcct gtaacctcaa caatttggga aggcagatca cctgaggtcg 49260 ggagctcgag accagcctgg ccaacatagt aaaaccctcg tctctactaa aaatacaaaa 49320 ataaattaaa aattagccaa gcatagtggt gcatgcctat aatcctggaa actcaagagg 49380 ttgaggcagg agaatcactt gaacttggga ggcggaggtt gcagtgagct gagatcgtgc 49440 cactgcactc cagcctccag cctgggcgat gacagagtaa gactccatct caaaaaaaaa 49500 aaaaaaagaa ggacttgaga ggatttccat tagccatcac caaccttgag gccgtccatc 49560 gtccatccat tggccacggc cacccaccgg ctggggagga gaaacctctt ggccatgtaa 49620 gcccgcagcc ccctcccagg gcagcatcat tcctcactgc ggtccaggtc cccaacccca 49680 gctctgtgag tcctcagaaa gcgagggccc ttgttgcttc agcctcctcc ttcatcctgc 49740 agaacacgcc agcctccctt gtgagcatct ccaagccacc gtaagatctg ggatttgctt 49800 taggttattt tgcccataac ccagaggctc atgaaaaatg tttttcccaa aacaaaagaa 49860 cactcttcac ccaaagataa atgcgctatc tggcaagaga aattggaaaa cattgctggc 49920 tgtgttaaac tagtagtcta actttagccc ccaaggtacc agagctctgc gaggccagtc 49980 tcagtataca cgacatgtaa taatgtgggg atgggtggta acataccagg aaagaaggac 50040 caggcaatgt gattaatgac caggaacccc catggtcctg caaagaggtg ctttgagaca 50100 agttggggac tagctctccc agcccagcac ctgcccaccc cagttcagag ccattgccgt 50160 gaacactctg aaatccccgt ggggctttgc ctttgcagag agccagccct ggggcctcct 50220 cctccctgcc cagctccagc accatccctg gctcgctcac ccaaactcac cgcttcctcc 50280 gtcattcccc gcaaggagtg gatgacatca ctctttccgg cagccaggag ttgacctaca 50340 ttccacccgc cctcctgtct gggagactct ccaaaccccc cgctcctctc tccctgggag 50400 gagggaaggg ccccgctcac gatttttgtg gagtgacggt gccaggcccg ggtccagatg 50460 gtgcccccgc agcagctccc aggcactgcc tgcccctccc tgcagcgcag ggcacgctcc 50520 tgcctggcac gggccagggc ccctgtcatc cttcatgtgg ctgtcaggcc cccagctggg 50580 cctgccacgt ttcccagaga actggtgtta tctgggctgg gctctcccct ggaggtgagg 50640 cccggtgctg cctactaaca gttgtggtct ccaggggctt actagggact catccattca 50700 agaaaaaggg aaacttagct gaaaaggtgg ctgtggctct gtccttgctg gcagcagggc 50760 cagcttccag caagcaagtg agtgcgcccc atgtcaggcc gtgagagaag tcagggtctg 50820 agcagagggg ccagacagcc acacgggtga gccgggtagc aggtgggcct gccagatgaa 50880 atacgggata cccagttaaa cctgaatttc agataaacaa gggaatcgtt gttttttagg 50940 gtaagtatgt cccaaatatt tcatggaata tacttgtact aacaaaatca ttagttattt 51000 atctaaaatt caaaaaaaaa tttttttttt ttagagacag ggtcttgctc tgtcacccag 51060 gctgaagggc agtgcagtgg cacaatcacg gctcactgca gcctcaacct cctggactca 51120 agcgatcctc ctgcctcagc ctccgaagta gctaagatga caggtgctca ccaccatgcc 51180 ctgataaatt ttgtgttttt ttaaattttt ttgtagagat tggggggggg gtctcacttt 51240 cttgcccagg ctggtctcaa actcctgttc tcaggtaatc ctcctgcctg ggcctcccag 51300 agtgcccaga ttacaagcat gagccactgc accaggccta aaattcaaat gtaactcagt 51360 gtcctgtatt tttatttggg aaatctggca accattgtgg catggggcta ctgtggggaa 51420 atgactccaa gaggccagtg ggggccaggc atggtggctt atacctgtaa tcccagcatt 51480 ttgggaggcc gaggtgggcg gatcatttga ggtcaggagt ttgagaccag cctggccaac 51540 gtggtgaaac cccatctcta ctaaaatact aaaattagcc gggtgtggtg gcgggcgcct 51600 gtaatcccag ctactcggga ggctgaggca gagaattgct tgaacccagg aggtggaggt 51660 tgaagtgagc caagatcgaa ccactgcact ccggtctaga tgacaaagcg agattccatc 51720 tcaaaataag taaataaata aaggataaat atctggcaat atgttactga atcctccaag 51780 aggccagggg gtgtgtcacc tcttggggcg ccccaggggc ctggagaata ggttgattat 51840 ctctattttg gggagctgca ggctctgaga gaggctctgg ggtgggtgtt ggacgggaca 51900 gcatgaataa ggggccctgc ccttggggtc aggcacctca gggctgccag gtaaggccga 51960 tcttggcacc tgggagccca tgtactctca tctccgtccc tccctctatc acctgttggc 52020 tgttgacaat agcaacaata ataatagctg acgtttccgg agggcatgct ctgtgccaga 52080 cccagtgctg agccctcaag ggtaccagct cagcttgccc ttccctgacc cttgacagtc 52140 ctgccacatg gaaacagcca cttcctaggg ttacaggaca ccgactgatt ccccaaggct 52200 ggtcaccttc ctgcctttgc ctagcttgag gggtcagagg tttgaacccg actgtctggc 52260 caccgcgcta cctggtgctg cagcccagcc gtgacactca ccggccttta acccagcagg 52320 tgctccatgc cggttgctgc acacagagct cccatgcatt atccccttcc tcccttgctt 52380 ctttctgcaa acattgagca cctactgtgt gccaggcagt gtgttagaca tttaccaaaa 52440 attaaaccca gagaagtgac ttgctcaagg tcacctagcc aatcagtagc aaaacctggg 52500 taagaatctg gctgctgact cagcctctct ctctctctct ctctctctct ctctctctct 52560 ctgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtcc catggagcgt tcttgctgcc 52620 atctgaagag ctaaagccgt gggattctgc agtggggcag gggtggagag ggaacagccc 52680 tggtggcctg ggaggggtcc actggcctca tgggctggcc agcatgccct atctctatgt 52740 tcattattaa atcatccttt ctgatggatg agctgaaaag tgctgtgtcg ggggatcagg 52800 tggcccaggt gatggttttc tggtgagatt gatggttcct gagggtcaaa ttcagagagc 52860 gatcgcttgg gaaaattgat cccacagaag aaggggaaat atctgggctg gagtgcagca 52920 ggagcccaga ctgcccgccc aggtccagat ccaggcagag gctggtgcca ggagggcacg 52980 tggcaaaggg ggcttctttc ttcttctgtg gctgcatttc cttggctgtg gctgggccac 53040 agaattggta agcagggcca tgggcagcag gcatgggggc atctggctta gtggcccctt 53100 tcctggcctt ctttgtcccc atggaatgga cgcgaagcca gcactgagag agacgcaggc 53160 agcaggtggc tgtgagatcc agctctagtg ccatgcagcc ccgagtgcca agcctgcttc 53220 ttccacccac agccctggcc cttgacccat ctgagcctcg cattctcacc tgtaaagtgg 53280 gaaggacagt gccttctgcg ttttcacgag gatttgttta ataatgcatg gcgtctgtcc 53340 acgtaggagc actcagcaaa ttatttctat gtgcttgctt atttatttca tttacttcat 53400 ctcccgaggg ccttccagaa tagggcagag aaatcacaga aggcaggcag cctgaggcag 53460 ggaggggaag ggtgtgcctg tgtctggggg agctgtgggg tggctgcagt tccaggagcc 53520 tgagtctatc caagagccag cacactgaga ctcttcaggc tctgcccact gcctgcccac 53580 ttcctaaagt ggggttcacc agctgtgtgg ccttgggcaa gttgcttaac ttctcttgcc 53640 tcatttcctt gtctgtgaaa tagagatagt catagtatac tctgcataag gttcctgtga 53700 agaggtgata acttcacttg ttgaaagctc tgaggatccc tggctctagg agctcctgag 53760 tataagaaat ggaaaactgg catgtcctag gcacctgttt gtctcatgca agagctttat 53820 agaccgtctc ccacttgatc cttccaacaa ctccatgagg caggtgttac tgccatcctt 53880 attttacaga ttagaaaaca ggccaagtga aattcagcaa ctttcctgag gtcacacagt 53940 cgttggcaga acatcccagg ccagtggggc ccaggggatg gggttaccat ctctcagtca 54000 cccagaaaga caaaaggaag gcacacaaac cccagtgggc accgctctgt gccagggctt 54060 ttgtttcacc ccaaccgtga tgagtgtggg tgatgtggcc ggtgtggtcc atatcgctcc 54120 tcagggccag tgtcactggt gtgcgtggca gcctgtggca tacacaagat attgtttccc 54180 gctcttcagg tgagaaaagc gagactcagg ttggctaaga atttgtgcag gccacacagc 54240 tgtgtgcacc atgagctggg cagaagccct gcccaccagc accatggggg ctcccggctc 54300 ctgccacaca ggccacccgg gagtgcagac actaagtgtg gctctgaatc gagctgcttg 54360 gattcaagtc ctgcgtctgc cccttaccag ctgtggaacc tcaggcagct cacttcacca 54420 ccccaagtct cagtttcccc atctgcacaa cgaagataat aatgacatgt cattcagggg 54480 attgctgtga agggctaatg ttctaattcg ggtggcactc tcagaacagt tcctcatgca 54540 aagtgagcac tcacgcatca gctgtctacc caggagactt cctttgaggc acaatgtgat 54600 agcgttttgt ttttttgttt ttttttgttt ttctggtttt tttgagacca agtgttgctc 54660 ttgtccccca ggctggagtg caatggcatg acctcggcct actgcaacct ccacctgttg 54720 ggttcaagcg atcctcctgc ctcagcctcc cgagtagctg ggattacagg cgcatgccac 54780 cacacccagc taatttttgt atttttagta gagacgggat ttcaccatgt tggccaggct 54840 ggtctcgaac tcctgacctc aggtgataca cccgcctcgg cttcccaaag tgctgggatt 54900 acaggcgtga gccaacgcgc ccggccccaa tgtgataggt ttataaaaat aggaaaacaa 54960 atctctgaag atttttagga gagatactgc aagaaaagcc tggaagctgt aagcccttcc 55020 ctgtttccac acatcccgat cattcattca ctcacagctt tacccagatg tgattcacac 55080 gttgtacaat ccacacatgt aaagcgtaca attcagtcgc ttttaggtta ttcacagagt 55140 tgtgcaacta tcaccacagc agactttaga acatttccat caccctaaaa agacactctg 55200 gccgggtgtg gtggcacacg cctgtaatcc cagctacttg ggaggctgag gcaggagaat 55260 cacttgaacc caggaggcag acattgcagt gagctgtgat cgtgacacta cactcagcct 55320 gggtgacaga gcaagactct gtctcaaaac aaaaaaaaaa aagaaaaaaa aagtcatcta 55380 cctatcctag acattttgtg taaatgaaat tatacaagat ggctgggcac ggtgcttcat 55440 gcctataatc ccagcacttt gggaggccca actgggagga tcacttgagg tcaggagttt 55500 aagattagca tggccaacat ggcaaaaccc catctgtact aaaaatacaa aaattagcta 55560 gatgtggtgg tgggtgcctg taatcccagc tacttagcag gctgaggcag gagaatcact 55620 tgaacccagg aggtggaggt tgcagtgagc caagatcata ccactgtact ccagcctggg 55680 tgacagagca agactctgtc tcaaaaaaaa aaaaaaaaaa gaaagaaaga aagaaattat 55740 acaatatgta gtctttcatc actgaccgct ttcacttggc ataatgtttt caaggttctt 55800 ccatgtcata gtgtggatca gtatttcatt actttttctg gctgtatagt attcattgcc 55860 tgcttacaca ttttgttttt ctgttgatgg atattgggtt gttcccacct tttgactatt 55920 attagcaatg ctgctatcaa cattcatgta cacattttgt gtggacatgt tttcgtttct 55980 cttggttata tacctaggta gaattactgg gcaactctaa gttcaccttt tgtagaactt 56040 ccagaccact ttccaaagca gctgcacaat tttacattcc caccagcagc gtatgagggt 56100 tctgatttct ctgcatcctc accagcaggt gattatccgt ctttttgact ctgcctatcc 56160 tggtgagtgt gaagtggtat ctcattatgg ctttggtgtg catttccctg atggctgtaa 56220 tgttgaacat gttttcatct gcttcttggc catttgtatg ccttcttcgg agaaatgtct 56280 gtgctgatcc tttcctcatt ttaaaaactg gattatttgt cattttatta ttgagttata 56340 agtgttcatt agatgttcta gatataagtt cctttttagc tatgtcatga cttgcaaatt 56400 tttctcccat tctgtgggtt gtcttttcac tttcctgaca gtgtcctctg aagtacaaaa 56460 atatttagtt ttgatgaagt ctaatttatc tatttttttt tcttctgttg cttttgcttt 56520 tggcatcctg tctaagaaac cattgcttaa ttcaaggtca tgaagatttg ctgctatgtt 56580 tccttcttct tttttttttt ttttttgaga cagagtctcg ctctgtgctc aggccagagt 56640 gcaatctcag ctcactgcaa cctctgcctc ctgggttcaa gtgattctca tgcctcagga 56700 cctcccaagt agttgggatt acaggcaccc accaccacac ctggctaatt tttgtgattt 56760 tagtagagac ggggtttcac catgttgacc aacttcaact cctgacctca ggtaacctgc 56820 ctgcctcagc ctccgaaagt gctcagatta caggcgtgag ccaccgcacc tggctcccta 56880 cgtttccatc tgagagtttt ctagtttgca gctctttgat ccattttgag ttaattttta 56940 tatgtgatgt gaagggtcca acttcattct ttttacgtgg gtctcccata ttatttattt 57000 atttgtttac ctaataattt ctttaaatta atatacttta aaaatttggt ttcacttagg 57060 cagtattttt gtgatcccag gtcttatgag tctgacatta aaaaaaacat actgtgtatt 57120 caaaaacaaa taatagcctg tagagctgtt ttacagtcca tgcgcccatc tcccccagtc 57180 atctcgtaca tcccactttg ggagccagtg ctgatcatga tgagttttat ggggagggag 57240 agtgtagcag gggctgattt gaggtagggg ttgtgaaagg cctccccaaa gaagtggcat 57300 ttggcctaga atctgacacc acctctaaat attagctcta ggagaagggg cagagcctgt 57360 agtacattcc aggcagaggg aacagcatgt gcaaaggccc agagaaaagc aagatcagaa 57420 catctgctgg acagagacat ggagagagag acaaagagac aggagaagac ggagacatgg 57480 agagaggggc actgagagag ccagagaggc caagaggtca tacacaaaca ccatgtccac 57540 acacaccgac acagaggcag taccacccac agtgacctgc aaaagtcaga gagaccagaa 57600 gcacctgcat tgaccaggtg ccatgtgtgt gccagccttg ccagcctttc cccacacagt 57660 gccagctcct ccctgcagcc ctgctagaca gggcaattct ctcctttgga agaggaggca 57720 ctgtgcttgt tctggggctc agccagcgag ttgaagaggc cgggacatct tctcctgttc 57780 ccgaggaaga caggactgat aggaggggct ggccaggatg gagcctgggc agagccagct 57840 ggggagggac gtctggattt gggtcaggag aaaccaactg tatgactttg ggcgacttct 57900 ccctaccagc accacccagc ctgtccagct ctgacatcca atggctacct attatcactg 57960 ttacaatatg cttcttggat tcggccggtc ttctatgcat ctttactaag ccaaggtcaa 58020 tgttatcacc caaagttgat ggcaatcttt tctttcggta gctgatatct aaaaatatcc 58080 cttcctcagg ccagcagtgc ggagcacagc cccggttccg tacagctgag gtgttcctct 58140 ccagccagct caggggggtg ttagatagga attcagaagt tgcgaattaa aacctcccca 58200 ggtcagattt tgcagacaaa ctcttgttag acaaagtcag acaggtttct tccctgcagg 58260 tcttgtcaga gcctttaatc tgctgagatg tattatgacc ctcagtggag tgaggtagga 58320 tcaaggagca gatgtcaggg gatttggaga gcatcatatg cttgaccaaa aaggtttaag 58380 cacagaaact ttctgtgcca aggaccatct ctgggatctg gcatctccag aaagaagggc 58440 cgcccgtacc aataggtgcc tgctgtcccc ctctgtgcct ttcccagagc taagcacata 58500 gcagtcctgc agcacgcatg tggcaatgga gggatgagaa tgccagggaa agagtgaaca 58560 ggctttttaa tgctctattt atttcagctt ggtgttccag taaaacctcg gcagggttag 58620 tgtccaggct ctcaggggaa gatggagtta aaatcacaca gacttcagcg gtggctagtg 58680 ctgctggcca gggctcttgc tctgcctcag aattctgttc cagagaattc cagagacgtc 58740 cttcgtcctg ggaactgagc atcacggcac agtggataca tgtaacctaa agcggtgggt 58800 tcctgagtgc cccctctccc acggcccacc caggacctgc aggattctct cctcctcctg 58860 ggaggaaagg cgtcagctca gaaactcact gccttctcca ctctggcctg acctcatgtt 58920 tctaaataac atttctaaaa catggacttt aggccagtcg caatggctca cacctataat 58980 cccagcactt tgggaggctg aggtgggcag attgcttgaa cttcaaccag gagtttgaga 59040 ccagcctggg caacacaggg agaccctatc tccacaaaaa ataaaaatga aattagccag 59100 gcatggtggc acgcgactgt ggtcccagct actcgggagg ctgaggaggg aggattgctt 59160 gagcccgaga ggcagaagtt gcagtgagcc gagattgtgc cacggcactc cagcctgggt 59220 gacagagtga gactcggtct caaaaagcaa aaagactcca ttgcctggat ttaccataat 59280 ttccctaacc attctgcagg ataattcgag gacagagaga agaccccaag gaggaaggca 59340 gccctggtta ccaaagctgg cagatggggg ttagctggaa gccccagggc tggtggacgc 59400 aggggccgct gtttccccac ccagatcctt gctctggaag gcggccccca ggggaccctt 59460 cattcccact cagacaggga cagaggcggg acagagccga gggaggaggg ctcagatgaa 59520 gcacctggca ggactgagat atgagggagg ccggatgcga ggagggagct ctgcagcctg 59580 tggtgtccag gaggatttgg ggagtgtgag gtgagaaaac aaaaagcgtc acccctccca 59640 gtggaagggg agcatgaaga gagaagaaaa tgccagttac acatcctcaa aacaatctct 59700 gaatggacga gagccagtca gggggaaacg gaagttgcag tgagccaaga ttgtgccacg 59760 gcactccagc ctgggtgaca gagtgagact ctgtctcaaa acacaaaaag atgccgcaca 59820 ccccaggcgg gacgggtggg cccaggtgcc ctgccctggt ccaggcctct attcgcagga 59880 tctcactgat ctctccctgc ccaggctttt gtctcccaga caaaccagtc tccatgaagc 59940 agccacagcg ttataaaata tggcccagag caggacacgc ctaaccagtc aaaggcttgc 60000 agagtaaaat cccgcctccg tctcctggtc tggcctcctc caccccccag cctcattgca 60060 gacctcacgg gtggaacttc tttcagccct agggctttcc tcatgctctt gcctctttct 60120 agaaggttct ccccttctgg cccggcaact cttgatcctc cttcaggtct tagtttaaaa 60180 ctgttcttcc tggaaactgt ggactcccgt gatgccttct tctttgcaca acccgtgggc 60240 tcttttaaca gttgaacact ggaagaggtg tgtgattcgt attgttataa ttaatagact 60300 ttatttttag agcagtttta agtttacaga aaattgagca gatagtacag aaagttccca 60360 tttccccacc cccctgcaca gtttccccta ttttggagta tatgtgttac aatgatgagc 60420 taacactgat acagtgtcat tcactagggc ctgttattta cattaggact cactctgtgt 60480 tggacacttc agtgggtttt gccatatgca taatgccaca tatctaccat tgtggcatca 60540 taaagaatgg tttcaccgcc ctaaaaatcc ctgtgtgcca cctatttatc ctccctccct 60600 gtcccctcca atcactgatt ttgttcattg tctccctgct agacccgaag caccatcagg 60660 tcagggagcc atctgctttg ttgacattat actcactgtt cccagctcag agcccctgcc 60720 acataacagg tgcctgataa atatttttct ttgcatattt taataaaaat aggattctac 60780 taaacccatt gctctgcaat ttgctttttc caaatattga caatatatct tggaaatctt 60840 cccatatcag aatatagagc acactctgtc tctctttcac tttttattat ggagaatttc 60900 caacacaaaa gaagatggtg tctgccatga tgaacctctg tgtacctctc acccgactgc 60960 agttaccaac tagtgaatct tcttgtttca tctgtacctc tgcccatcag ataatttcat 61020 ctgtaaatat ttctatgtgt atctctctct gctttttttt ttccttttga gatgtagtct 61080 cgctctgtct cccaggctgg agtgcagtgg tgcaatggct cactgcaacc tctgcctcct 61140 gggttcaagc gattctcctg cctcagcctc cccagtagct gggattacag gtgcaccatc 61200 acacttggct aattttgtat ttttagtaga gatggggttt caccatgtcg gacaggctgg 61260 tcttgaactc ctgacctcaa gtgatctgcc tgccttggcc tcccaaagtg ctaggaatac 61320 aggcataaac caccatggct ggcccttttg ttttgttttg tttttgtttt tgttttgttt 61380 gtttttgttt tgttttgttt tgtttttttt ggagacagag tcttgctctg tctcccaggc 61440 tggagtgcag tggtgcaaac atggcttgct acagccttga actcctgggc tcaagggatc 61500 ctcctgccct agcctcttga gtagctagga ctgcaggcat gtgccaccac actggctaat 61560 ttttttattt tctgtagaaa caggatctta ctatgttacc cagtctggcc tcaaattcct 61620 gggctcaatt gatcctcctg cgtcagcctc ctaaagtgct tggattatag gtgtgcacca 61680 ccacgcctag cctgtgtggt tctctaaaag ataaggactt taaaaaacat aaccacaata 61740 tcatcatcac acctagtaaa cattagtatc taatataggc aatgtccaaa tttccagtta 61800 tctcataaat atacgttcca tttgtttgcg tgtttgattt tacaggatgt ttgaaccaag 61860 gaccagagga gcttcacttc tgccattaat tggtatgctt ttgaggtttc tcttgctcta 61920 ggtccatcct ttttccgtat caattttttc tccacgcaac tcatctgttg gaagaagtgg 61980 gtcattactg ccggagtttc ctcgagtcca gatcttgcgg atggcatccc ctggtgtcgt 62040 tcagggtgat gctctgtcct ctgtctttcc tgtgcgctca cagctgggtc tagaggcttg 62100 atctgattca ggttcagttg ctttggcttc gggtgggggt gtgttcttct agagacgctc 62160 actgtctgct ggcctctcag tgggaagttc tgggctggtg cggctcagtg cctggagcta 62220 tgcattcatc agggactgca aattctctcg tgaaatgctt ctataaaaag aagcttcccc 62280 tcatcaactt tcggttaccc cgaggtacag tttatatagg acaggcagga taaatgcttg 62340 attctttccc tttatttacc agttttcaga ataatgagtc gcctataaat atttgaatga 62400 atggatgaat aatacacctg tgaatgaact gacgggggtg tgggagttgg gggttctatc 62460 tgttgccctc aagggcgtgg ctgtgggcca caacctgaca gcagaggtcc agcctgaagc 62520 caggtgcctt tctacacaat gaagtgcagc ccatggccaa gtctctgtct acaccaggtg 62580 ctggcagcag cctctgtcac ccatcaaccc acatcagtca aaggctaggg tgatcagaag 62640 ctgcattact aagaatctag catctgggac aaggcagtat catcactctc cccaactgag 62700 atgtgaggaa tccttgaaac cagcatcaga gcagagagga gagccgcgca gtgactgcag 62760 gtgtggcctt tggaacacgg cgttgatctc tctgcaggaa ggggaatcaa ggagtttctg 62820 gcctaaaggt tgggctggtg gcctccaggg tttcttcctg ggcagcccaa caccctcctg 62880 ggcccctcct gggaggcgct cctttcccca gaggccaggc caggctgccc acaagctctc 62940 tgacatctct gccctctcgg tgtctcccca ggtgcaagtg caacctgcat gccaacctgt 63000 gctccatgcg cgagggcagc ctgcagtgcg agtgcgagca caacaccacc ggccccgact 63060 gcggcaagtg caagaagaat ttccgcaccc ggtcctggcg ggccggctcc tacctgccgc 63120 tgccccatgg ctctcccaac gcctgtacgt gccatgcccc ggggccacga gcccacatgg 63180 ctataatctt ccctgcccgt caatcccagg agctgtggat catacacacg cacacaaacc 63240 tgcacacagg cacatacgtg tgcacatgca tgcaaacgtg cacacagaaa catacgagca 63300 tgcatgcaca ggcatgggca cacatatgaa tgcaaaaaca cgtgcatgca cagaaacaca 63360 cgtgcgtgca tgcaccccca cacacacacc ttgttctaca gctcccaaat gccaggtctc 63420 ataacaagtc cctctagcat acctgcatcc tgctgaatgc taagctgccc ttccagccct 63480 ggtccacagg gaaacccgag aggagctgct cagcagcatt cctgcaaccc ttcgccttct 63540 tgaccctgaa ggctggcagg tggcccccat gggatggcag ggagtgatgg ggtgggaccc 63600 ccacttcagg tgaggggatc agtagcatca tccctgatca taagcatctc tggggtgttt 63660 ggagcgagcc accaaggcca agtgctgcgt gttcagcact cacctccatc ctcagagcaa 63720 cccctgggaa ctgagcttcc gttatccctt tttacagatg tgtcctctac ggcctgcacc 63780 agagtccccc cgcacgtgct ctctgcccac ccctctcctg tcctcgccca gccatgccag 63840 ggagccatcc tcagggcctg cccactcaca tctgcatcat agaccccctt ctgaggacca 63900 cccacccggg cgcgctagcg tagtccacac tgtctccatg aaatcagaat gccaggaagc 63960 ccctgggctg caagtggaga aggccacaga ctgcccctgg ggtgggctct ccctgacccc 64020 caccactgcc actttacggc cgttctcaag tgtgtggttg gtgtccgagg ccctcctagg 64080 cactttgtgc atctcgcttc accctcacac agccccgcag ggtggagtcc ttattacggt 64140 cccttctcca gatgagcaga ctgaggccca gcgaacctcg gggccctccc aggtttcaca 64200 gtgagttgca tgccaacgcc agggcttagg gcagctactg gatctgatgc tcagaccagg 64260 cctgggcagt ggcctcctgc accccatctg ggcatcctcc ctcgacgggt gaaagattta 64320 tgtgacttta ggctgatcaa agctgagagc cacgtgcaga ggccatgaca ggcatgtcac 64380 gcgtgtgcta cagcaggcgg tgagacaggc ctttgaaggg gtgacttggc aggcacccga 64440 cagcactctc gggtcttcaa aggcacaaag agcactccgg gggctgacag cccactccag 64500 ccgctgcctc ctcccagctt cctgtcccca tctctttgtg gtccaaaccc tttcctgagg 64560 tctctcttta gtggccgtca ctctctccct gactcacaaa tttgctgccc tttcgtctgt 64620 cctgagggcc gctctctctt ccctcctctc tgtctcagtt ctctccacca tcacaccctc 64680 cttttttttt ttttcttaaa gataagtctc tcactctgtc gtccaggctg gagtgcagtg 64740 gcgcagtcat ggctcactgt aacctcaacc tcctgggctt gagcgatcct cccacttcag 64800 cctcccaagt agctgggact gcaggtgcac accaccaggc ccagctaatt ttcgtgtttt 64860 tttcagagaa aaggttttgc catgttgccc aggctggtct cgagctcctg agctctagta 64920 accctcctgc cttggcctcc caaagtgctg ggattacagg catgagccac cacgtctggc 64980 catgtctggc ttttttcttc cacttgcccc ctgcgcctgg agggttctgc ccatctctgg 65040 ccacctgaga ctcttacctg ccagtcacac ctaggaggat ccactgtccc caccctcacc 65100 cccagtcacc acctccagtc tagccagcga tggatagaca ggcctgtagg ggctgggcag 65160 ctgggtcttc cttacttagg ggagactcct gagctggccc cacctcctgc ttccctggga 65220 gtccccggga attgcctttg aggcccccaa gccccaggaa ggaggggttt cttctggcat 65280 ttgcagggtc acaggtgagg ctggaggcgc tgctgtcctc agcacccaag tctcctgcct 65340 tctctggggt gccagcagga aacagcccaa agagacacag aggctaattt tgccctcacc 65400 ctgcccctac cgtgacccct cctcagtaag tggcaccgac acccacgggg ccaagtgcaa 65460 gtctgggggt caccttgact ggagaccctc ctcccgccac gttctttgaa cttccctcca 65520 tccgctccaa gtctctccca atgccatcct cagccctgca gcagccctca ctcccgatgc 65580 cttcccacct cctcaccact ctgcccccac ctggccagcc catcaccctc cagggcccaa 65640 cttggagccc ccaggacctc cccgtgccct gcctgatgtc ccgcctgtcc ccacagagcc 65700 tcacttggtc accacccagt cctggccctt gcttactgtg gctgcacccc gaggtgtcct 65760 cagggtctag caggtggctg cccagacatg gaggtagagg aaggagtggg tggggatggg 65820 cttgtcctcc caggcctccc tgcctgtcct gctggccaca gccttggctt gcccaggaga 65880 agcccatggg ccacacatcc cactgccaat cccacagcgt cctttctcgg gaacaccgtg 65940 gggaaagctg tggcaccagc tccttccttt tgcaactctg atgaatctca cccagggatt 66000 tcaaggcccc tggtcacacc aggatcatag gcctccccca tcccctggac acacagagac 66060 acacctggat tcaggtcagg cctcgcccac tctcggctat atttctcccc aagccgtgtg 66120 tcctcagctg tagaatcagg accataagga agttccctca tagggttctt gtgaggacgg 66180 cacgatttac gtaggggatg ctgacaccgt gcctggcacg tgggacgcac tccacccgcg 66240 gcagccgctc ccatggcttc tcagtgagtt ttccagccac actgcacttc ttagacagga 66300 acactccata cgatgtccct gtcctgcact ggatggccca aaaatctgaa ataagaggag 66360 gagtgcgtgt gaagctccca gtggagcgtt tggcacctgt ccagcatgtc cccaagggca 66420 agtcacggct ctgagattca gtgtctcctt ctgcaaaatg ggccaatagt ggttcctccc 66480 tcccagggct gaagtgagga tgaaatggga taatccaccc ccgtccccac accctgcagg 66540 tcatcatcat tgctagcagt tgtgtggtgg agcaggtgct cttgagggag cgacacctcc 66600 aggtgctccc ctgccctgct ggcccctctg cagggaggtg acacccaggc cccttcccct 66660 ggggcagcca gctcacgccc gtctctctcc cacaggtgcc gctgcaggtt cctttggcag 66720 taagtacacg cctggggagg gtggccaggg cccccactgc acgagcctct ttgcatgtcc 66780 tggaaaaagc tggagagaaa aaaggggctt cagtgtcccc tctgggactt gggcctattc 66840 actccctcct ctaattacac cccatctgct tctccacctc tcccccctcc acctcccccc 66900 ctccacccat ccccacttca catcatatgc catgtgtcat gtgtcatttt gctgtggcct 66960 gtggcccagc aactctcagg ctctcccagg agctccatca gtgctgcttt ggaaaacggg 67020 acaggacttt ttgcaggtct cttggcccct gggtgggctc cctgctcctc ctgccaccca 67080 cgccacttct ctcacctgga tctgggagag cagtctctcc tgccagtcaa gagtggggtg 67140 accttccccc accaggggca gaatccaccc cctagcctaa ccatgggggc agcctccctc 67200 tgggcagcct ctgcagccag cttgtcccag ggctctgctc gtccaggtca gctcaggtcc 67260 caggggagtc ggaccaggga ggggcatctg caggaggtgg gggtcctgag agttccccag 67320 gagggcgagg gcgacatggc gcccacaggt tatcagtaaa tgtcatcgag actgtcccca 67380 gacactcaca gggtgccagg cacggtctct cctttcagcc ttgcaaaccc ctccccctgg 67440 gaggtcgcca tctgctctgc gaggcagcag gagaggactg gccaatgtca aagagccagc 67500 cgggagcaga ccccaaatct cagagatgct tctggggtgc accgtcaccc tccaccaggg 67560 ctctgtgggg ccccacatcc cacccaagtt gtccctcccg gacccagggg gcccctggct 67620 gggaagccag tgagccgaga gggcgccaga aagaagctgg accctgcagg gacgctggtc 67680 tgcacagccg tcgtaagttg cttctctgtg gtgtccccac cccggcaacc ccccaaccct 67740 ctcttgcttt tcccatctct caccaggcat cagcaggtcc cagaaagacc ccgaccccaa 67800 aggccctgtg gccactgcgg ccaccacagc catgacaggg gcccctacta ctcctgtccc 67860 ctccacgtcc actgcctggg cccccatggc gcccagcacc ccacagccca caggtgggtg 67920 ccagggtaca gcgacccctg tcatcccacc ctctcctgct tctagcctgg gtccctgcct 67980 ctcttggggt gggagggtcg gcagccctgg gcagagagca ggggcttggc tcttagaata 68040 gagacgctag aaccctagag ctgggaggcc acaggccaaa ggggcttgag gacacctggg 68100 tcaacctgtt cctgagccca gccaggggat tcagggatca gttcagcttc caaagtcgtc 68160 ttcctcctgc ccttcaagcc attgcttgga agggctccca gaccattgtg gccagacggc 68220 tgcaggaact gagaggaaag gtgctggggg cagcgaggcc atcctgacat gcagccaaag 68280 actggcctta tctcccaatg gtgcttctgc ctccgtggtc cctggagccc cgcccacacc 68340 ctgtccccac ctggccccca gggcctctct gtccttagcc cctcagcagc acaccggtgg 68400 gatggatgga gcagggttag cccagaaagc aaatgtctct gatcagcagg gcaaagggag 68460 cctctggagc tgagtttgga caccgtgggc tgctgggaat gtggaggctg tgtgtgtagt 68520 gcaaggccag gccagggcca gacgtcctgc cccctcaggg gtctgccaca gacaggcatg 68580 gaaacctgat tctcgctccc ctccaacgga gggattcacg tgtattcaag gctgggggtg 68640 ctggagtggg cctctgctct cacctggact cacctgggga gtatccctgc actctgtgca 68700 gtgcaggtgc caggggtctg aaaggattta tccttcccag agggcaccag gaagacgatg 68760 accaagggga attcttcctg gtcccagcca gggaggggtg ctccaatagc ctgccacacc 68820 ctgtcccccg ccaccctgca gggaggacct ggtggggact cctggcccct tgggtagtgc 68880 cctggccctc catctctctg atccaaggag acctgcccca ctgatccttc ccccttgggg 68940 ggtggcattt ctaaagggca gagtcccctc catcagctcc tgcctcggcc tgttgctggg 69000 tggacactca ggctccccag acaggggcaa atgctgagag aaagacctcc tccttcctag 69060 gccatccaga gcagctcccc tgggggcagc acaccccacc tctttctaca tccttccttt 69120 tctgcaggag gcatttacag gaggcagggg ctagccaaaa gattggagga tttccgggaa 69180 gcctcctgac ccaggaatcc tctttggggt ggaagacatg ggtcactctg agaattctgg 69240 acttcagaca taggttggcc cagccacaag ggacctgtgc tttgctgatg agcctgtggt 69300 gggcagacag aagcaaaaac agtggtggtg ggtgctgtgc ctgtctccaa acaggggttt 69360 ggctgggagg ccagatactc tccatatcac atgtgcaagt gcacacatgc acacacacac 69420 atgcatgcac acacacaggc atgcacacgc acatgtacac acacacacac acagaggaat 69480 ccatttgcag agctgcttct gacttggtgc cagggcagcc gtgggaggct gggcagattg 69540 tgcaaagttg ggaattaaag aggaaaagtc agaggccaga gtgggaaatg caggggagtt 69600 gagggtcccc aggaccccct cagtgagcag aaggcacacc ctccctctcg gcaagacagt 69660 gctgctctgc accctcagcc ctgtatcaag aagcaggaca ttaggggagg aggtggctcc 69720 aatgtgacag ccagtggccc ctacagccca catctagggg ctcctccctc ctcttcagca 69780 actgaagccc ctgtccagag cccccattaa tgaaaacgat cattgcagta gctgagggtg 69840 agttctcctg ggctgtgctc gtatcattgt atcatcatat cattgtattc tgggctcaca 69900 gctccgtgag atggaggctg ttattttcct agtcccacag gtgaggggat cgaggcttag 69960 gaagaagcag ctggatttta tgatatgtaa attacacctc aatcaagctg tttcagaaga 70020 aaaaaggggc agctgctcaa ggtctcagaa ttatggagag gcacgggcag gatttgaact 70080 cagggctcgc caactcagcc acccaaagct attgtcctga ggcctccagg ggctatgagg 70140 tagagctatc tttttttttt ttttttgaga tggagtttcg ctcttgtcgc tgaggctgga 70200 gtgcaatgga gcaatctcag ctcactgcaa cctccgcccc cccaggttca agcaattctc 70260 ctgcctcagc ctcccgagta gctgggatta caggcacctg tcaccatgtt cagctacttt 70320 ttgtcttttt agagagacag ggtttcacca tgttggtcag gctggtgttg aactcctgac 70380 ctcaagtgat ccacccgcct cagcctccca aagtgctggg attccaggcg tgagccaccg 70440 cacccggcca agtagtgctg tctccaaggc ctggcttgca gggcttccca gttccaaagg 70500 agcagaccgg gcttccatgg ggccttggca cagcacacag gccatggcga gaacttgctt 70560 cccacacacc tgagtgtgtc cctgggcagc caagccagga ctccctccct ccccaagacc 70620 ctggtccctg aaagatcctg aatacccccg agtgcctccc aacaggtgct tcgggctctt 70680 tgaacagagt ccagctgggc ctctgaactc ctgggccaga tgtttctccc gcctgccaat 70740 gtcaagctgt ctggaggaca gcgctgcggg cggaaaacgc cgctggagac actaatcctt 70800 tcctgggctg ggccacggag gatggaggga gacaggctct gaagcaaatg ccttcagggc 70860 tggctttctc atggctctaa ttaagccctt gccaatttgg gcctggcggc ctcatcttcc 70920 cactgaacat catattaaag tcaattcatg tccaaagctc cccgctccca gctggaaagt 70980 cttccgcact tgttagctgg tagcttttcc ttttctttcc ccacagccac cgttgtgtat 71040 aatcccttca agaagcggaa aacagcagcg ctcccctgtc cctctgggtt tgtcctttga 71100 aatttgggca cagggcagtt ctttgccagc cctgcctgcc tgccttgctg gctgtgtgtc 71160 ccgttagtct acgggctgag cgttgtgtca ttggttcatg ctggggtccc tggtgaaaat 71220 gggccaggcc aggggtcagg aaggtagaag ggcagtgatc agggaagcag gtcagatgct 71280 ggggaaggct ccggtccctg gattgcggct ggacaggaag gacaccttcc aggacacttc 71340 tggacacatg taagatcttg gccggaacac atgtcccact tcgcagccat tagccagaga 71400 catcagctca gagaggtctg ggcccagagg cgggacctgg tctagctctg tccttcagtc 71460 agaacgggga cggcacaggg agtgtagaag ggtctcgctg aagaatatgc agattctcag 71520 gcatgggttc acctctcatc tatcgggctt taagtctgca tgtgccctcc acaggctgaa 71580 atagtgtaga tgctgcctat gtagtagatt tggacccaat tcctttggcc agtgtagaca 71640 gagcctctcc ttatagtgct gctgcttcta aggggcctgt ggggtgcggg gctgtgatgc 71700 ctcagtatgt acccagcttc cctcagcacc accccctcgc ataacttggt ttcttctctt 71760 cttcccccca agagtggacc aggccatcta cggctgcccc tctctcgagc aggtggtccc 71820 aggtggcctc ccgtgcagaa ggtatggggg ggcaaggcct gtgatgggcc tgagaccccg 71880 gggaagcgcc ctcttagact cgtaggcccc tccctctgta gtggaagtag caggtgtgca 71940 tggtggggac ctgaggttgg aggggggccg caggaaccaa ctgagggcac gggtgtagaa 72000 tgtcggtgcc tggggagctc tagggcacag tggtgaggga gcggcctggt agagcaggtc 72060 taccagctct gcccccaagc tcacctgctt caagaggttc catgtggcac ccccacgcca 72120 agcccttcca ccagcactcc ctccgagggc ttcggagtct ggtagaggcc ccgcctccca 72180 cgacaggaac ccccctctcc agctgccctt gctcacagga cacctgggca gttgctggat 72240 cagagagtca gagggggctt cctgcaggag cgggggccat gagacctcgg agggtggact 72300 gtggtgggtg aagggagaag gcagcacatt ccaggccgca gggccagccg gggcaaaggc 72360 ttggcagtgg gatggcaggg agcctgacaa agtggaaaat gtgtgggtta aaggagggag 72420 ggcggggtcc tggaagacac tgacatcctc ctgctacgtg ggaggagaca cagggctcat 72480 ctgtagccat agacagacat gccaaggaaa cgcgcaggcc tgcccgactc tccagaaggg 72540 aaattgtccc tggccccagc tcaccaagcc tgggtgggga attagggcct gaggtctagg 72600 gaacaggtga gctgttcctt ccagctcaca tgttcaaatt tcctccagcc ccagctctga 72660 gcagcgagca gggctttgag cgccctctac tggcaggaag ctctggcgct ggaagcatgt 72720 ttagagaggg tctgaggctc ggttcctaga aacctggagg acctgggcct ggtgtcctct 72780 gtggtgatgg agacagagct ggcgggagcc atcgcttccc taccctgggc caaccagggc 72840 accacagacc cccagaggga agccaaggta gtgacgatcc cgggacagtg gcctgctcac 72900 ccacagatag ggcgttgggg tcccagcggg attctgggca gtggaaggca ggtgccgtcc 72960 gtgttcctgg cttgacagca cttgcgagtg ggactccagg gacagcgaag gattcacttc 73020 ggctggagca ggaagagtgt ttcagaaagg aagggagatg ccaaagtcct taaatgccaa 73080 gtttagtctc tgggtttgat gctccaggaa gtttggagag gcggtgggga gagcaagaga 73140 cgggcgtggt gtgcaatgtg atgtcaatct atctaaaaac agtttggctt ccaagaaggt 73200 cttagcaggg cgcgggggtg tcaggggtta cagaagtcat ttggaggatt aatccagcca 73260 gatgtgtcca tggtctcaga gaggggacca agggcagggc tgatttgcaa gcttgggatg 73320 tgctgtgttt ccttcaggaa ggggccccac ctccctgggc tcttcgagga gaggggctgt 73380 gtgatttgag gccagagggg cctctccctc cctcacatct gagcaggcga caaggctgcc 73440 tgccctagag ctggcccagg gcggctcgga agcctttgct gggctcttcc ctgggcagtg 73500 ggaccatgac agacgaaaga acctgtttct catctctcca agctgtgggc acccctgccg 73560 ctgcccctgc ccctgccaag ggctacaaac ttttccagct caagcccaaa tctcctcaag 73620 tgatgcctat tgaagaattc caaggtaaga ggatggacct ggggccccat cagccctccc 73680 tgacacctgt tccccatccg ccgctggaaa aagacggtgc aggatagagg accgatgcct 73740 ggctccgaaa accctcctgg agtagctggg tcaaggttaa actgagtctc tcttccctac 73800 aggcctccct ccccaaggga gctgggagca ggtatgagtc agaagccaac ttgggcacag 73860 tgggcaggcc acacagcagg cagagcagat gccagaaata gcccatcccg gctcccctgg 73920 gaggtgtggc cctggggctc gtgttggttg aagcagaatc tgggacacac gggtcaccga 73980 tgctgctctt tgggacactt agaggatgcc tcatctcctc attatctctg gagggacaaa 74040 gtgaaggggg caggactagg tggcccacag gtgggagtgc ccaccatctc tcctgggcac 74100 aggctgtttc tctagtctcc catgcccttg accactgggt cagtccctca tcccatcaca 74160 aaagggaagc tgggtcctct agagatacac agatggtgtt tcaagagggt ggccgttgtc 74220 cttccttgtt cgggggcagc cacattggct ttcttgctgg agggtgggtg ggtgggtgag 74280 tactgtgtcc cttcgtagga acatcaaggg atgccccccc attcttaggg atggtgacct 74340 tcctcaccaa atcctccatt gacaatgtgg gattcacctc caatccctga gagccttgcc 74400 ccaggcagtc acgggcttgt ctggtccttg gagcggagct ggttaggcag gggtcagcct 74460 gagaaccacg taggggtggg gtgcaggagg cggcaggaca tggtggtggt ggtccttggt 74520 atgaaaccat gtgcttccag gagcagcgag tcagaagccg ggccaggacc agggggaggc 74580 atgcaggttc ccagggctcc tgctttaaag tggcactcac tcttagcatc ctgcaaaaca 74640 atcaaacttg cagaaagctc aggctaataa gaaagggtct ggcaggtggg cgttttcctc 74700 ccagccatct tccaaagcag catgggcagg agctcctggc ccattgcatc ttgtccagcg 74760 tccatccatg cattcatcta cccgaggata ccacggcgag cgccgtgaac ccaggcgtcg 74820 ccctccccca gtgcacagcc aggtggcatg accctgccct ccttgcatga atcactttct 74880 aatcaccccg gcatgtgggc atccttcagc gagcgcttgg ccctggtgcc cagccaggca 74940 ttagcaggag ctgcccactg gccctccctg gttccctgcc cacagggcca ggtgggaatc 75000 cctgggctca gcctactcag gttctcctct gggctcaaag cagggaggcc tctctcttcc 75060 tgaatccgat ggaagggtgg gaggcctagg gcaccttccg gtaccttttc caaagatgcc 75120 ttcctccgtc cctgcatgac ctggggtgag tccttcctcg ccctgtccct cagtttccct 75180 gaatgctcgc tgaccattgg tatttctccc acttggccgg cccagactgc gaatgctacg 75240 gtcactccaa ccgctgcagc tacattgact tcctgaatgt ggtgacctgc gtcagctgca 75300 agcacaacac gcgaggtcag cactgccagc actgccggct gggctactac cgcaacggct 75360 cggcagagct ggatgatgag aacgtctgca ttggtgagag ggcacggaca cggcacaggg 75420 aacttgctgg aatgcgtgca gggtgcactg ccctgcgagg tggcctctgg ggccccctgc 75480 atcagaatca cctggggaga ctgtgggaat tctaactcca gggccctctc cagttgagca 75540 tctctaagga cagaaagctc cagaaactgc tctattagta acctaccctt gcggttctcc 75600 ggtaagtttt gcactggagt tgcaaaactt accagtggcc cttccctctc tgggcaactg 75660 gaggggacac tgacccttcc tggctccaaa gagctgtgac tctggcaggt ggcaggcact 75720 cagtggcaga ggccactgag catctgtctg gggctggtgt gtgggggggt ccccctccat 75780 agctcctttc cagaaaggtg gaggagcagc ctatccctcc tcctgcaggg gcccagttgg 75840 gggccaaaag atcgccttgc tgcgtgcatt tgtgcaagtc ccttcccgtt cctgggcctc 75900 agcttcctca ttcatcaaat tgggaggcag atcagatcaa aggttttcag ctcttttttg 75960 tggctgaagc ttttcttcaa atgctttacc agcccaggtc cagctataaa gctgctcttc 76020 acccctggtg ggcacccagt ctgctttctt ccaagttcta ctcaaggact ggcttttggg 76080 tagagaagga agtccatcag ggccctgggc ctgggcaaag accaaagcca tgaccgccaa 76140 ccaaaacgca ccagcctgga atggttgccc ctgtcgtcag tagaggccag gtctcggcct 76200 caggggctgt cccccaaccc tgcccagcca ggccccttgg gacaccatca cccatccccc 76260 acccagcagg aggctctggc tgcccagagg aggggctcct gcaaagctgg agctgtcggt 76320 ctgaattctg gcggcagcct tcagataatt ccatcaactc taagtgatca aagccgctga 76380 cgtcacaggg ggccagctgc agggacaggg cagggccttt ggatccaatt agaggtgccc 76440 acaccctggc accctcctcc tctccctggc tctccctgcc tccaccccga gagccagcac 76500 tgagctgcaa ggtttctcag ggtggacgat attcaccctc tcccacagag ccccaaggca 76560 accaactggg cccaccccgg gagcaggaat aggctgttcc tccactcccc tgcaaaggag 76620 ctatggaggg gggccacccc acaacacagc agccccagac atgctcagtg gcctctgctg 76680 agtttctgcc acctgtcgga gtcatagctc tttggagatg ggaaggacag cgacccctct 76740 agttgcccag agaggggaag gggctgaccc aggccacacc agtgccaggg cggggaaggt 76800 ggggctggga cgtgtttgat cccaaggaag gaagccagag tcttctctcc aggcctggcc 76860 accctgggaa gtccccacct gccgtccagc cgcgggctca cgtggaccca gtgtggggag 76920 catcccctgg ggagtgtgga gatgctccct gcgaggccgg gagagtgggg gtccgagaag 76980 acggcgccca cacgtagccc tgaccgcgcg cccgtgcccg tgtccgtcca gagtgtaact 77040 gcaaccagat aggctccgtg cacgaccggt gcaacgagac cggcttctgc gagtgccgcg 77100 agggcgcggc gggccccaag tgcgacgact gcctccccac gcactactgg cgccagggct 77160 gctaccgtga gtgcgcgccg tcccccgtgg gcggggcctg cggaaagggg acggggcagg 77220 accgaggcag tgggcggggc ctagtgggac ggggcagggg cggtggactg ggcctagcaa 77280 gacggggcag ggccggggaa gtgggtgggg cctagtggga cggggaagag gcggtgggcg 77340 gggctcgcga gacggggcag ggccggggca gtgggtgggg cctagatgag agcggggcag 77400 ggttgggata gttggcaggg gcctggtgag atggggccga cccgggggcg gtggacgggg 77460 cctagcgaga cggagctggc aggtgggcgg ggacaggatg ctgctgaggt ccggggccgg 77520 gccgaggggc gggtccaaga gctcggggcg gggcctgatg cgacctgagg cacggtggtg 77580 cctggtggga actacgagaa agaccgagct ggggttggtt ggaaaggtat ttgcggggac 77640 agagggaggg aggctgtcca agtcggcgtt agccgcgggc acagggtgaa aggaggctcc 77700 aggcgcgtgg aacagcacgt gcacagctct ggagactgca ggcgcgtctg aagaacagca 77760 ccgaggccag tggggcgggg agagaggggc agcggtggga ggcagccggg ggccagtatc 77820 tcgcccgggc gccgtcaccc tccgaggggg gacgtttcgc acccagcgcg cctggagcct 77880 cctacatccc cggcccagac ggcgcccccg ggatctcgca caccctgctt cgcaggagct 77940 cggaggttgg cggggggacc gggccacccc ccgtgctgac cgccccctcc gcctgcagcc 78000 aacgtgtgcg acgacgacca gctgctgtgc cagaacggag gcacctgcct gcagaaccag 78060 cgctgcgcct gcccgcgcgg ctacaccggc gtgcgctgcg agcagccccg ctgcgacccc 78120 gccgacgatg acggcggtct ggactgcgac cgcgcgcccg gggccgcccc gcgccccgcc 78180 accctgctcg gctgcctgct gctgctgggg ctggccgccc gcctgggccg ctgagccccg 78240 cccggaggac gctccccgca cccgggagcc gggggtcccg gggtcccggg gcggggccgg 78300 cgtccgaggc cgggcggtga gaagggtgcg gcccgaggtg ctcccaggtg ctactcagca 78360 gggccccccg cccggcccgc gctcccgccc gcactgccct ccccccgcag caggggcgcc 78420 ttgggactcc ggtccccgcg cctgcgattt ggtttcgttt ttcttttgta ttatccgccg 78480 cccagttcct tttttgtctt tctctctctc tctttttttt tttttttttc tggcggtgag 78540 ccagagggtc gggagaaacg ctgctcgccc cacaccccgt cctgcctccc accacactta 78600 cacacacggg actgtggccg acaccccctg gcctgtgcca ggctcacggg cggcggcgga 78660 ccccgacctc cagttgccta caattccagt cgctgacttg gtcctgtttt ctattcttta 78720 tttttcctgc aacccaccag accccaggcc tcaccggagg cccggtgacc acggaactca 78780 ccgtctgggg gaggaggaga gaaggaaggg gtggggggcc tggaaacttc gttctgtaga 78840 gaactatttt tgtttgtatt cactgtcccc tgcaaggggg acggggcggg agcactggtc 78900 accgcggggg ccgatggtgg agaatccgag gagtaaagag tttgctcact gctgcctcca 78960 cggcctgttt tctttctgtg ttggggacgg tgggcaggtg tggggcttac agaggaatcc 79020 acaacacagc cttaaagaaa cggtttccct actggggcca ccatttccct gggcctttct 79080 gtggattcca gcaggcagtg ccccctcccc gcaggcttgg ctggcagagt tttccacccc 79140 gcggccaggc tgcaggtgcc ccacctgtta ggagcctccc cacactgaaa ggctgcctcc 79200 ctcctttccc aaaaaagaaa tccggagtgt attggccctt ttctacagaa gtccaaggga 79260 aatgactcag ggagaatcct agcagaggtt gaatccaatg ctctgattta tactgtgtct 79320 cggtggccac ctccgatgga tgtgtcatct cagacctgtt gcagccggag cctcaagtcc 79380 aatatcagat gaagctgaac ccacaattcg gccaccgcct ccttccagag tttcagatgg 79440 ccaggtgggc agaggcgggc agtgcagaga ccccagacgt gccggccctg tcctccctac 79500 cttctcaaga ttaggaaggg gtgctggagg ggacaggggc agcttgggag tggtgaggaa 79560 gctcctagat tcggggctca tcccctgggg cctctgattc agaggatcca gcagttctcc 79620 catctccgct tggtgtctcc agccctgggg ccacacttcc ccctcggtcc agcctcctgt 79680 ccacctatgt ttatttcaga gcagtgccgg gggtccggtc ctggttgcta actgctgcca 79740 ctgctccacc tgcaggtgct cccagcactg gcttctgcca ccacacctgt tctttcccag 79800 ctgcgaggtt tagacctggg tccttccctt gagtccccaa agctaagcta agaccaagtg 79860 gaacaaactt ggccttgggg acagcaggag attacaacac agaaaaggag ggggaggcac 79920 aacgggacac tgcataggac tcacagtgtc ccgagcccac acaccagccc ctcctggcct 79980 cctctctctg ctcccacccc cagcaccctg ctgacccgga agtgccttcc gacaggccct 80040 gcatcctcct gcagctggcc catctctacc ctcacattct tccttacgca cagaacccca 80100 ctgcctggga cccaaagtgc ccagataaaa taaaacacct ctctggggct tcttgtggat 80160 aggagtggcc aggggacaca gctctgggca gtgagatgta agcaggactg atgggtgggc 80220 ttccagaaag ttcttaaaag tcatcccttc ctccacgccc cacaaagcct cagttgtcca 80280 agtttgtggc tctggttttt ctctctcatc cctccctctg ctcttcagtc agcaggatgg 80340 ggaaggagcc ttcttgagac actgagcata acagtgtcac cctcaggata gtgaagggtg 80400 gagccggggg tggaagttgc agagcctggg acacctgcct tggctgcaac ctctgcactg 80460 cttttattta tctacttatt tttatagagt tgaggtctca ctatgttgcc caggctggtc 80520 tcaaactcct aggctcaagt gagcctccgg ccttggcctc ccgaagtgct gagattacag 80580 gcatgagcca ccgcaccacc tgcctgtctt actgtgtgag aaaaaaaata aacggtgatg 80640 tgattaaaac actagaattt gggttttctg ttccatgcac actttccaag ttcttggccc 80700 tgcctgattg gcatccgggc cccctgagcc ctctaaggcc agagagagac tgaaacccac 80760 ccttccttgg ccgcagcccc ccatggtgac cctcaagtca ccaggaagag gaatgtccat 80820 gactcaggcc gaggagtcca cctctgtcca gaacaggact gcccctgcct tctagtgagc 80880 acagggcagc tgagcagaac tcaccccaga gaaacagcag cgctggccgc agtcggtaaa 80940 cagcaggcat ttcctccta 80959 4 510 PRT Mus musculus 4 Gly His Tyr Asp Val Cys Lys Ser Leu Ile Tyr Thr Glu Glu Gly Lys 1 5 10 15 Val Trp Asp Tyr Thr Ala Cys Gln Pro Glu Ser Thr Asp Met Thr Lys 20 25 30 Tyr Leu Lys Val Lys Leu Asp Pro Pro Asp Ile Thr Cys Gly Asp Pro 35 40 45 Pro Glu Ser Phe Cys Ala Met Gly Asn Pro Tyr Met Cys Asn Asn Glu 50 55 60 Cys Asp Ala Ser Thr Pro Glu Leu Ala His Pro Pro Glu Leu Met Phe 65 70 75 80 Asp Phe Glu Gly Arg His Pro Ser Thr Phe Trp Gln Ser Ala Thr Trp 85 90 95 Lys Glu Tyr Pro Lys Pro Leu Gln Val Asn Ile Thr Leu Ser Trp Ser 100 105 110 Lys Thr Ile Glu Leu Thr Asp Asn Ile Val Ile Thr Phe Glu Ser Gly 115 120 125 Arg Pro Asp Gln Met Ile Leu Glu Lys Ser Leu Asp Tyr Gly Arg Thr 130 135 140 Trp Gln Pro Tyr Gln Tyr Tyr Ala Thr Asp Cys Leu His Ala Phe His 145 150 155 160 Met Asp Pro Lys Ser Val Lys Asp Leu Ser Gln His Thr Val Leu Glu 165 170 175 Ile Ile Cys Thr Glu Glu Tyr Ser Thr Gly Tyr Ser Thr Asn Ser Lys 180 185 190 Ile Ile His Phe Glu Ile Lys Asp Arg Phe Ala Phe Phe Ala Gly Pro 195 200 205 Arg Leu Arg Asn Met Ala Ser Leu Tyr Gly Gln Leu Asp Thr Thr Lys 210 215 220 Lys Leu Arg Asp Phe Phe Thr Val Thr Asp Leu Arg Ile Arg Leu Leu 225 230 235 240 Arg Pro Ala Val Gly Glu Ile Phe Val Asp Glu Leu His Leu Ala Arg 245 250 255 Tyr Phe Tyr Ala Ile Ser Asp Ile Lys Val Arg Gly Arg Cys Lys Cys 260 265 270 Asn Leu His Ala Thr Ser Cys Leu Tyr Asp Asn Ser Lys Leu Thr Cys 275 280 285 Glu Cys Glu His Asn Thr Thr Gly Pro Asp Cys Gly Lys Cys Lys Lys 290 295 300 Asn Tyr Gln Gly Arg Pro Trp Ser Pro Gly Ser Tyr Leu Pro Ile Pro 305 310 315 320 Lys Gly Thr Ala Asn Thr Cys Ile Pro Ser Ile Ser Ser Ile Gly Asn 325 330 335 Cys Glu Cys Phe Gly His Ser Asn Arg Cys Ser Tyr Ile Asp Leu Leu 340 345 350 Asn Thr Val Ile Cys Val Ser Cys Lys His Asn Thr Arg Gly Gln His 355 360 365 Cys Glu Leu Cys Arg Leu Gly Tyr Phe Arg Asn Ala Ser Ala Gln Leu 370 375 380 Asp Asp Glu Asn Val Cys Ile Glu Cys Tyr Cys Asn Pro Leu Gly Ser 385 390 395 400 Ile His Asp Arg Cys Asn Gly Ser Gly Phe Cys Glu Cys Lys Thr Gly 405 410 415 Thr Thr Gly Pro Lys Cys Asp Glu Cys Leu Pro Gly Asn Ser Trp Tyr 420 425 430 Tyr Gly Cys Gln Pro Asn Val Cys Asp Asn Glu Leu Leu His Cys Gln 435 440 445 Asn Gly Gly Thr Cys Gln Asn Asn Val Arg Cys Ala Cys Pro Asp Ala 450 455 460 Tyr Thr Gly Ile Leu Cys Glu Lys Leu Arg Cys Glu Glu Ala Gly Ser 465 470 475 480 Cys Gly Ser Glu Ser Gly Gln Gly Ala Pro Pro Arg Gly Ser Pro Ala 485 490 495 Leu Leu Leu Leu Thr Met Leu Leu Gly Thr Ala Gly Pro Leu 500 505 510 5 260 PRT Human 5 Leu Tyr Lys Tyr Phe Tyr Ala Ile Ser Asn Ile Glu Val Ile Gly Arg 1 5 10 15 Cys Lys Cys Asn Leu His Ala Asn Leu Cys Ser Met Arg Glu Gly Ser 20 25 30 Leu Gln Cys Glu Cys Glu His Asn Thr Thr Gly Pro Asp Cys Gly Lys 35 40 45 Cys Lys Lys Asn Phe Arg Thr Arg Ser Trp Arg Ala Gly Ser Tyr Leu 50 55 60 Pro Leu Pro His Gly Ser Pro Asn Ala Cys Ala Ala Ala Gly Ser Phe 65 70 75 80 Gly Asn Cys Glu Cys Tyr Gly His Ser Asn Arg Cys Ser Tyr Ile Asp 85 90 95 Phe Leu Asn Val Val Thr Cys Val Ser Cys Lys His Asn Thr Arg Gly 100 105 110 Gln His Cys Gln His Cys Arg Leu Gly Tyr Tyr Arg Asn Gly Ser Ala 115 120 125 Glu Leu Asp Asp Glu Asn Val Cys Ile Glu Cys Asn Cys Asn Gln Ile 130 135 140 Gly Ser Val His Asp Arg Cys Asn Glu Thr Gly Phe Cys Glu Cys Arg 145 150 155 160 Glu Gly Ala Ala Gly Pro Lys Cys Asp Asp Cys Leu Pro Thr His Tyr 165 170 175 Trp Arg Gln Gly Cys Tyr Pro Asn Val Cys Asp Asp Asp Gln Leu Leu 180 185 190 Cys Gln Asn Gly Gly Thr Cys Leu Gln Asn Gln Arg Cys Ala Cys Pro 195 200 205 Arg Gly Tyr Thr Gly Val Arg Cys Glu Gln Pro Arg Cys Asp Pro Ala 210 215 220 Asp Asp Asp Gly Gly Leu Asp Cys Asp Arg Ala Pro Gly Ala Ala Pro 225 230 235 240 Arg Pro Ala Thr Leu Leu Gly Cys Leu Leu Leu Leu Gly Leu Ala Ala 245 250 255 Arg Leu Gly Arg 260 

That which is claimed is:
 1. An isolated peptide consisting of an amino acid sequence selected from the group consisting of: (a) an amino acid sequence shown in SEQ ID NO: 2; (b) an amino acid sequence of an allelic variant of an amino acid sequence shown in SEQ ID NO: 2, wherein said allelic variant is encoded by a nucleic acid molecule that hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; (c) an amino acid sequence of an ortholog of an amino acid sequence shown in SEQ ID NO: 2, wherein said ortholog is encoded by a nucleic acid molecule that hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; and (d) a fragment of an amino acid sequence shown in SEQ ID NO: 2, wherein said fragment comprises at least 10 contiguous amino acids.
 2. An isolated peptide comprising an amino acid sequence selected from the group consisting of: (a) an amino acid sequence shown in SEQ ID NO: 2; (b) an amino acid sequence of an allelic variant of an amino acid sequence shown in SEQ ID NO: 2, wherein said allelic variant is encoded by a nucleic acid molecule that hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; (c) an amino acid sequence of an ortholog of an amino acid sequence shown in SEQ ID NO: 2, wherein said ortholog is encoded by a nucleic acid molecule that hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; and (d) a fragment of an amino acid sequence shown in SEQ ID NO: 2, wherein said fragment comprises at least 10 contiguous amino acids.
 3. An isolated antibody that selectively binds to a peptide of claim
 2. 4. An isolated nucleic acid molecule consisting of a nucleotide sequence selected from the group consisting of: (a) a nucleotide sequence that encodes an amino acid sequence shown in SEQ ID NO: 2; (b) a nucleotide sequence that encodes of an allelic variant of an amino acid sequence shown in SEQ ID NO: 2, wherein said nucleotide sequence hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; (c) a nucleotide sequence that encodes an ortholog of an amino acid sequence shown in SEQ ID NO: 2, wherein said nucleotide sequence hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or3; (d) a nucleotide sequence that encodes a fragment of an amino acid sequence shown in SEQ ID NO: 2, wherein said fragment comprises at least 10 contiguous amino acids; and (e) a nucleotide sequence that is the complement of a nucleotide sequence of (a)-(d).
 5. An isolated nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of: (a) a nucleotide sequence that encodes an amino acid sequence shown in SEQ ID NO: 2; (b) a nucleotide sequence that encodes of an allelic variant of an amino acid sequence shown in SEQ ID NO: 2, wherein said nucleotide sequence hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; (c) a nucleotide sequence that encodes an ortholog of an amino acid sequence shown in SEQ ID NO: 2, wherein said nucleotide sequence hybridizes under stringent conditions to the opposite strand of a nucleic acid molecule shown in SEQ ID NOS: 1 or 3; (d) a nucleotide sequence that encodes a fragment of an amino acid sequence shown in SEQ ID NO: 2, wherein said fragment comprises at least 10 contiguous amino acids; and (e) a nucleotide sequence that is the complement of a nucleotide sequence of (a)-(d).
 6. A gene chip comprising a nucleic acid molecule of claim
 5. 7. A transgenic non-human animal comprising a nucleic acid molecule of claim
 5. 8. A nucleic acid vector comprising a nucleic acid molecule of claim
 5. 9. A host cell containing the vector of claim
 8. 10. A method for producing any of the peptides of claim 1 comprising introducing a nucleotide sequence encoding any of the amino acid sequences in (a)-(d) into a host cell, and culturing the host cell under conditions in which the peptides are expressed from the nucleotide sequence.
 11. A method for producing any of the peptides of claim 2 comprising introducing a nucleotide sequence encoding any of the amino acid sequences in (a)-(d) into a host cell, and culturing the host cell under conditions in which the peptides are expressed from the nucleotide sequence.
 12. A method for detecting the presence of any of the peptides of claim 2 in a sample, said method comprising contacting said sample with a detection agent that specifically allows detection of the presence of the peptide in the sample and then detecting the presence of the peptide.
 13. A method for detecting the presence of a nucleic acid molecule of claim 5 in a sample, said method comprising contacting the sample with an oligonucleotide that hybridizes to said nucleic acid molecule under stringent conditions and determining whether the oligonucleotide binds to said nucleic acid molecule in the sample.
 14. A method for identifying a modulator of a peptide of claim 2, said method comprising contacting said peptide with an agent and determining if said agent has modulated the function or activity of said peptide.
 15. The method of claim 14, wherein said agent is administered to a host cell comprising an expression vector that expresses said peptide.
 16. A method for identifying an agent that binds to any of the peptides of claim 2, said method comprising contacting the peptide with an agent and assaying the contacted mixture to determine whether a complex is formed with the agent bound to the peptide.
 17. A pharmaceutical composition comprising an agent identified by the method of claim 16 and a pharmaceutically acceptable carrier therefor.
 18. A method for treating a disease or condition mediated by a human secreted protein, said method comprising administering to a patient a pharmaceutically effective amount of an agent identified by the method of claim
 16. 19. A method for identifying a modulator of the expression of a peptide of claim 2, said method comprising contacting a cell expressing said peptide with an agent, and determining if said agent has modulated the expression of said peptide.
 20. An isolated human secreted peptide having an amino acid sequence that shares at least 70% homology with an amino acid sequence shown in SEQ ID NO:
 2. 21. A peptide according to claim 20 that shares at least 90 percent homology with an amino acid sequence shown in SEQ ID NO:
 2. 22. An isolated nucleic acid molecule encoding a human secreted peptide, said nucleic acid molecule sharing at least 80 percent homology with a nucleic acid molecule shown in SEQ ID NOS: 1 or
 3. 23. A nucleic acid molecule according to claim 22 that shares at least 90 percent homology with a nucleic acid molecule shown in SEQ ID NOS: 1 or
 3. 